-
1
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A., Lombardo, F., Dominy, B. W., Feeney, P. (1997). Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Advanced Drug Delivery Reviews, 23, 3-25.
-
(1997)
Advanced Drug Delivery Reviews
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.4
-
2
-
-
0035273557
-
Estimation of aqueous solubility of organic molecules by the group contribution approach
-
doi:10.1021/ci000152d
-
Klopman, G., & Zhu, H. (2001). Estimation of aqueous solubility of organic molecules by the group contribution approach. Journal of Chemical Information and Computer Sciences, 41(2), 439-445. doi: 10. 1021/ci000152d.
-
(2001)
Journal of Chemical Information and Computer Sciences
, vol.41
, Issue.2
, pp. 439-445
-
-
Klopman, G.1
Zhu, H.2
-
3
-
-
0037072566
-
Nanoparticles in cancer therapy and diagnosis
-
doi:10.1016/S0169-409X(02)00044-3
-
Brigger, I., Dubernet, C., Couvreur, P. (2002). Nanoparticles in cancer therapy and diagnosis. Advanced Drug Delivery Reviews, 54(5), 631-651. doi: 10. 1016/S0169-409X(02)00044-3.
-
(2002)
Advanced Drug Delivery Reviews
, vol.54
, Issue.5
, pp. 631-651
-
-
Brigger, I.1
Dubernet, C.2
Couvreur, P.3
-
4
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
-
doi:10.1023/A:1016212804288
-
Amidon, G. L., Lennernas, H., Shah, V. P., Crison, J. R. A. (1995). A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharmaceutical Research, 12(3), 413-419. doi: 10. 1023/A: 1016212804288.
-
(1995)
Pharmaceutical Research
, vol.12
, Issue.3
, pp. 413-419
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.A.4
-
5
-
-
0035997323
-
A biopharmaceutics classification system: the scientific basis for biowaiver extensions
-
doi:10.1023/A:101647360163
-
Yu, L. X., Amidon, G. L., et al. (2002). A biopharmaceutics classification system: the scientific basis for biowaiver extensions. Pharmaceutical Research, 19(7), 921-925. doi: 10. 1023/A: 101647360163.
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.7
, pp. 921-925
-
-
Yu, L.X.1
Amidon, G.L.2
-
6
-
-
77956251066
-
Biopharmaceutical classification of drugs
-
Available from Accessed: 18 Jun 2012
-
Gothoskar, A. V. (2005). Biopharmaceutical classification of drugs. Pharmacy Review. Available from: http://www. pharmainfo. net/reviews/biopharmaceutical-classification-drugs. Accessed: 18 Jun 2012.
-
(2005)
Pharmacy Review
-
-
Gothoskar, A.V.1
-
7
-
-
62649137652
-
Biopharmaceutics classification system: validation and learnings of an in vitro permeability assay
-
doi:10.1021/mp800122b
-
Thiel-Demby, V. E., Humphreys, J. E., et al. (2009). Biopharmaceutics classification system: validation and learnings of an in vitro permeability assay. Molecular Pharmaceutics, 6(1), 11-18. doi: 10. 1021/mp800122b.
-
(2009)
Molecular Pharmaceutics
, vol.6
, Issue.1
, pp. 11-18
-
-
Thiel-Demby, V.E.1
Humphreys, J.E.2
-
8
-
-
79959906965
-
The BCS, BDDCS, and regulatory guidances
-
doi:10.1007/s11095-011-0438-1
-
Chen, M., Amidon, G. L., Benet, L. Z., Lennernas, H., Yu, L. X. (2011). The BCS, BDDCS, and regulatory guidances. Pharmaceutical Research, 28(7), 1774-1778. doi: 10. 1007/s11095-011-0438-1.
-
(2011)
Pharmaceutical Research
, vol.28
, Issue.7
, pp. 1774-1778
-
-
Chen, M.1
Amidon, G.L.2
Benet, L.Z.3
Lennernas, H.4
Yu, L.X.5
-
9
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system
-
doi:10.1016/j.ejps.2006.04.016
-
Pouton, C. W. (2006). Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. European Journal of Pharmaceutical Sciences, 29(3-4), 278-287. doi: 10. 1016/j. ejps. 2006. 04. 016.
-
(2006)
European Journal of Pharmaceutical Sciences
, vol.29
, Issue.3-4
, pp. 278-287
-
-
Pouton, C.W.1
-
10
-
-
33644881395
-
Stabilization of solid dispersions of nimodipine and polyethylene glycol 2000
-
doi:10.1016/j.ejps.2005.12.009
-
Urbanetz, N. A. (2006). Stabilization of solid dispersions of nimodipine and polyethylene glycol 2000. The European Journal of Pharmaceutical Sciences, 28(1-2), 67-76. doi: 10. 1016/j. ejps. 2005. 12. 009.
-
(2006)
The European Journal of Pharmaceutical Sciences
, vol.28
, Issue.1-2
, pp. 67-76
-
-
Urbanetz, N.A.1
-
11
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
doi:10.1021/ja02086a003
-
Noyes, A. A., & Whitney, W. R. (1897). The rate of solution of solid substances in their own solutions. Journal of the American Chemical Society, 19, 930-934. doi: 10. 1021/ja02086a003.
-
(1897)
Journal of the American Chemical Society
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
12
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
-
doi:10.1016/0378-5173(95)00122-Y
-
Liversidge, G., & Cundy, K. (1995). Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. International Journal of Pharmaceutics, 125, 91-97. doi: 10. 1016/0378-5173(95)00122-Y.
-
(1995)
International Journal of Pharmaceutics
, vol.125
, pp. 91-97
-
-
Liversidge, G.1
Cundy, K.2
-
13
-
-
46749104406
-
Bioavailability and bioequivalence: focus on physiological factors and variability
-
doi:10.1007/s11095-008-9645-9
-
Benet, L. Z. (2008). Bioavailability and bioequivalence: focus on physiological factors and variability. Pharmaceutical Research, 25(8), 1956-1962. doi: 10. 1007/s11095-008-9645-9.
-
(2008)
Pharmaceutical Research
, vol.25
, Issue.8
, pp. 1956-1962
-
-
Benet, L.Z.1
-
14
-
-
0025755129
-
Particle formation with supercritical fluids-a review
-
doi:10.1016/0021-8502(91)90013-8
-
Tom, J. W., & Debenedetti, P. G. (1991). Particle formation with supercritical fluids-a review. Journal of Aerosol Science, 22(5), 555-584. doi: 10. 1016/0021-8502(91)90013-8.
-
(1991)
Journal of Aerosol Science
, vol.22
, Issue.5
, pp. 555-584
-
-
Tom, J.W.1
Debenedetti, P.G.2
-
15
-
-
0035803697
-
Organic nanoparticles in the aqueous phase theory, experiment, and use
-
doi:10.1002/1521-3773(20011203)40:23<4330::AID-ANIE4330>3.0.CO;2-W
-
Horn, D., & Rieger, J. (2001). Organic nanoparticles in the aqueous phase theory, experiment, and use. Angewandte Chemie (International Ed. in English), 40(23), 4330-4361. doi: 10. 1002/1521-3773(20011203)40: 23< 4330:: AID-ANIE4330> 3. 0. CO; 2-W.
-
(2001)
Angewandte Chemie (International Ed. In English)
, vol.40
, Issue.23
, pp. 4330-4361
-
-
Horn, D.1
Rieger, J.2
-
16
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy: rationale for development and what we can expect in the future
-
doi:10.1016/S0169-409X(00)00118-6
-
Muller, R. H., Jacobs, C., Kayser, O. (2001). Nanosuspensions as particulate drug formulations in therapy: rationale for development and what we can expect in the future. Advanced Drug Delivery Reviews, 47(1), 3-19. doi: 10. 1016/S0169-409X(00)00118-6.
-
(2001)
Advanced Drug Delivery Reviews
, vol.47
, Issue.1
, pp. 3-19
-
-
Muller, R.H.1
Jacobs, C.2
Kayser, O.3
-
17
-
-
4544383493
-
Nanosuspensions in drug delivery
-
doi:10.1038/nrd1494
-
Rabinow, B. E. (2004). Nanosuspensions in drug delivery. Nature Reviews Drug Discovery, 3(9), 785-796. doi: 10. 1038/nrd1494.
-
(2004)
Nature Reviews Drug Discovery
, vol.3
, Issue.9
, pp. 785-796
-
-
Rabinow, B.E.1
-
18
-
-
0037312695
-
Nanosizing: a formulation approach for poorly water-soluble compounds
-
doi:10.1016/S0928-0987(02)00251-8
-
Merisko-Liversidge, E., Liversidge, G. G., Cooper, E. R. (2004). Nanosizing: a formulation approach for poorly water-soluble compounds. European Journal of Pharmaceutical Sciences, 18(2), 113-120. doi: 10. 1016/S0928-0987(02)00251-8.
-
(2004)
European Journal of Pharmaceutical Sciences
, vol.18
, Issue.2
, pp. 113-120
-
-
Merisko-Liversidge, E.1
Liversidge, G.G.2
Cooper, E.R.3
-
19
-
-
0035186701
-
A nifedipine coground mixture with sodium deoxycholate. II. Dissolution characteristics and stability
-
doi:10.1081/DDC-100107676
-
Suzuki, H., Ogawa, M., Hironaka, K., Ito, K., Sunada, H. (2001). A nifedipine coground mixture with sodium deoxycholate. II. Dissolution characteristics and stability. Drug Development International Pharmacy, 27(9), 951-958. doi: 10. 1081/DDC-100107676.
-
(2001)
Drug Development International Pharmacy
, vol.27
, Issue.9
, pp. 951-958
-
-
Suzuki, H.1
Ogawa, M.2
Hironaka, K.3
Ito, K.4
Sunada, H.5
-
21
-
-
0037151528
-
A novel particle engineering technology: spray-freezing into liquid
-
doi:10.1016/S0378-5173(02)00154-0
-
Rogers, T. L., et al. (2002). A novel particle engineering technology: spray-freezing into liquid. International Journal of Pharmaceutics, 242(1-2), 93-100. doi: 10. 1016/S0378-5173(02)00154-0.
-
(2002)
International Journal of Pharmaceutics
, vol.242
, Issue.1-2
, pp. 93-100
-
-
Rogers, T.L.1
-
22
-
-
1142309798
-
Rapid dissolving high potency danazol powders produced by spray freezing into liquid process
-
doi:10.1016/j.ijpharm.2003.11.003
-
Hua, J., Keith, P., Johnston, B., Robert, O., Williams, A. (2004). Rapid dissolving high potency danazol powders produced by spray freezing into liquid process. International Journal of Pharmaceutics, 271, 145-154. doi: 10. 1016/j. ijpharm. 2003. 11. 003.
-
(2004)
International Journal of Pharmaceutics
, vol.271
, pp. 145-154
-
-
Hua, J.1
Keith, P.2
Johnston, B.3
Robert, O.4
Williams, A.5
-
23
-
-
0037151563
-
Microencapsulation of protein particles within lipids using a novel supercritical fluid process
-
doi:10.1016/S0378-5173(02)00149-7
-
Ribeiro, D. S., Richard, J. B. P., Thiesc, C., Benoit, J. P. (2002). Microencapsulation of protein particles within lipids using a novel supercritical fluid process. International Journal of Pharmaceutics, 242(1), 69-78. doi: 10. 1016/S0378-5173(02)00149-7.
-
(2002)
International Journal of Pharmaceutics
, vol.242
, Issue.1
, pp. 69-78
-
-
Ribeiro, D.S.1
Richard, J.B.P.2
Thiesc, C.3
Benoit, J.P.4
-
24
-
-
22844436560
-
Supercritical fluid technology for enhanced drug delivery
-
doi:10.1517/17425247.2.4.747
-
Pathak, P., Meziani, M. J., Sun, Y.-P. (2005). Supercritical fluid technology for enhanced drug delivery. Expert Opinion on Drug Delivery, 2(4), 747-761. doi: 10. 1517/17425247. 2. 4. 747.
-
(2005)
Expert Opinion on Drug Delivery
, vol.2
, Issue.4
, pp. 747-761
-
-
Pathak, P.1
Meziani, M.J.2
Sun, Y.-P.3
-
25
-
-
43449094630
-
A novel bottom-up process to produce drug nanocrystals: controlled crystallization during freeze-drying
-
doi:10.1016/j.jconrel.2008.03.002
-
Waard, H. D., Hinrichs, W. L. J., Frijlink, H. W. (2008). A novel bottom-up process to produce drug nanocrystals: controlled crystallization during freeze-drying. Journal of Controlled Release, 128(2), 179-183. doi: 10. 1016/j. jconrel. 2008. 03. 002.
-
(2008)
Journal of Controlled Release
, vol.128
, Issue.2
, pp. 179-183
-
-
Waard, H.D.1
Hinrichs, W.L.J.2
Frijlink, H.W.3
-
26
-
-
0033805858
-
Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and "self-microemulsifying" drug delivery systems
-
doi:10.1016/S0928-0987(00)00167-6
-
Pouton, C. W. (2000). Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and "self-microemulsifying" drug delivery systems. European Journal of Pharmaceutical Sciences, 11, 93-98. doi: 10. 1016/S0928-0987(00)00167-6.
-
(2000)
European Journal of Pharmaceutical Sciences
, vol.11
, pp. 93-98
-
-
Pouton, C.W.1
-
27
-
-
0037123703
-
Microemulsion formulation for enhanced absorption of poorly soluble drugs: I prescription design
-
doi:10.1016/S0168-3659(02)00049-4
-
Kawakami, K., Yoshikawa, T., Mororo, Y., Hayashi, T. (2002). Microemulsion formulation for enhanced absorption of poorly soluble drugs: I prescription design. Journal of Controlled Release, 81(1-2), 65-74. doi: 10. 1016/S0168-3659(02)00049-4.
-
(2002)
Journal of Controlled Release
, vol.81
, Issue.1-2
, pp. 65-74
-
-
Kawakami, K.1
Yoshikawa, T.2
Mororo, Y.3
Hayashi, T.4
-
28
-
-
33847256524
-
A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymerosomes
-
doi:10.1016/j.ejpb.2006.11.009
-
Letchford, K., & Burt, H. (2007). A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymerosomes. European Journal of Pharmaceutics and Biopharmaceutics, 65, 259-269. doi: 10. 1016/j. ejpb. 2006. 11. 009.
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.65
, pp. 259-269
-
-
Letchford, K.1
Burt, H.2
-
29
-
-
34247642609
-
Targeted nanoparticles for cancer treatment
-
doi:10.1016/S1748-0132(07)70083-X
-
GuFX, K. R., WangAZ, A. F. E., et al. (2007). Targeted nanoparticles for cancer treatment. Nano Today, 2, 14-21. doi: 10. 1016/S1748-0132(07)70083-X.
-
(2007)
Nano Today
, vol.2
, pp. 14-21
-
-
Gufx, K.R.1
Wangaz, A.F.E.2
-
30
-
-
34547797860
-
Anticancer polymeric nanomedicines
-
doi:10.1080/15583720701455079
-
Tong, R., & Cheng, J. J. (2007). Anticancer polymeric nanomedicines. Polymer Reviews, 47, 345-381. doi: 10. 1080/15583720701455079.
-
(2007)
Polymer Reviews
, vol.47
, pp. 345-381
-
-
Tong, R.1
Cheng, J.J.2
-
31
-
-
14144250911
-
Recent advances with liposomes as pharmaceutical carriers
-
doi:10.1038/nrd1632
-
Torchilin, V. P. (2005). Recent advances with liposomes as pharmaceutical carriers. Nature Reviews. Drug Discovery, 4(2), 145-160. doi: 10. 1038/nrd1632.
-
(2005)
Nature Reviews. Drug Discovery
, vol.4
, Issue.2
, pp. 145-160
-
-
Torchilin, V.P.1
-
32
-
-
33845388144
-
Micellar nanocarriers: pharmaceutical perspectives
-
doi:10.1007/s11095-006-9132-0
-
Torchilin, V. P. (2007). Micellar nanocarriers: pharmaceutical perspectives. Pharmaceutical Research, 24(1), 1-16. doi: 10. 1007/s11095-006-9132-0.
-
(2007)
Pharmaceutical Research
, vol.24
, Issue.1
, pp. 1-16
-
-
Torchilin, V.P.1
-
33
-
-
41949100244
-
Drug nanoparticles: formulating poorly water-soluble compounds
-
doi:10.1177/0192623307310946
-
Merisko-Liversidge, E. M., & Liversidge, G. G. (2008). Drug nanoparticles: formulating poorly water-soluble compounds. Toxicologic Pathology, 36(1), 43-48. doi: 10. 1177/0192623307310946.
-
(2008)
Toxicologic Pathology
, vol.36
, Issue.1
, pp. 43-48
-
-
Merisko-Liversidge, E.M.1
Liversidge, G.G.2
-
34
-
-
1842559836
-
Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs
-
doi:1 0.1081/DDC-120030422
-
Hu, J., Johnston, K. P., Williams, R. O. (2004). Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Development and Industrial Pharmacy, 30(3), 233-245. doi: 10. 1081/DDC-120030422.
-
(2004)
Drug Development and Industrial Pharmacy
, vol.30
, Issue.3
, pp. 233-245
-
-
Hu, J.1
Johnston, K.P.2
Williams, R.O.3
-
35
-
-
0026730479
-
Further histologicalevidence of the gastrointestinal absorption of polystyrene nanospheres in the rat
-
doi:10.1016/0378-5173(92)90162-U
-
Jani, P. U., Florence, A. T., McCarthy, D. E. (1992). Further histologicalevidence of the gastrointestinal absorption of polystyrene nanospheres in the rat. International Journal of Pharmaceutics, 84, 245-252. doi: 10. 1016/0378-5173(92)90162-U.
-
(1992)
International Journal of Pharmaceutics
, vol.84
, pp. 245-252
-
-
Jani, P.U.1
Florence, A.T.2
McCarthy, D.E.3
-
36
-
-
0029938692
-
The effect of adsorbed poloxamer 188 and 407 surfactants on the intestinal uptake of 60 nm polystyrene particles after oral administration in the rat
-
doi:10.1016/0378-5173(95)04353-5
-
Hillery, A. M., & Florence, A. T. (1996). The effect of adsorbed poloxamer 188 and 407 surfactants on the intestinal uptake of 60 nm polystyrene particles after oral administration in the rat. International Journal of Pharmaceutics, 132, 123-130. doi: 10. 1016/0378-5173(95)04353-5.
-
(1996)
International Journal of Pharmaceutics
, vol.132
, pp. 123-130
-
-
Hillery, A.M.1
Florence, A.T.2
-
37
-
-
78649976662
-
Stomach-specific mucoadhesive microsphere as a controlled drug delivery system
-
doi:10.4103/0975-8453.59515
-
Rajput, G., Majmudar, F., Patel, J., Thakor, R., Rajqor, N. B. (2010). Stomach-specific mucoadhesive microsphere as a controlled drug delivery system. Systemic Reviews in Pharmacy, 1(1), 70-78. doi: 10. 4103/0975-8453. 59515.
-
(2010)
Systemic Reviews in Pharmacy
, vol.1
, Issue.1
, pp. 70-78
-
-
Rajput, G.1
Majmudar, F.2
Patel, J.3
Thakor, R.4
Rajqor, N.B.5
-
38
-
-
0342897023
-
Nanosuspensions for the formulation of poorly soluble drugs: I. Preparation by a size-reduction technique
-
doi:10.1016/S0378-5173(97)00311-6
-
Peters, K., & Muller, R. H. (1998). Nanosuspensions for the formulation of poorly soluble drugs: I. Preparation by a size-reduction technique. International Journal of Pharmaceutics, 160(2), 229-237. doi: 10. 1016/S0378-5173(97)00311-6.
-
(1998)
International Journal of Pharmaceutics
, vol.160
, Issue.2
, pp. 229-237
-
-
Peters, K.1
Muller, R.H.2
-
39
-
-
16244398708
-
Nanosuspension formulationsfor low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compound
-
doi:10.1081/DDC-52182
-
Langguth, P., Hanafy, A., Frenzel, D., Grenier, P., et al. (2005). Nanosuspension formulationsfor low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compound. Drug Development & Industry Pharmacy, 31(3), 319-321. doi: 10. 1081/DDC-52182.
-
(2005)
Drug Development & Industry Pharmacy
, vol.31
, Issue.3
, pp. 319-321
-
-
Langguth, P.1
Hanafy, A.2
Frenzel, D.3
Grenier, P.4
-
40
-
-
33645030096
-
Preparation and evaluationof nanosuspensions for enhancing the dissolution of poorly water-soluble drugs
-
doi:10.1016/j.ijpharm.2006.01.008
-
Kocbek, P., Baumgartner, S., Kristl, J. (2006). Preparation and evaluationof nanosuspensions for enhancing the dissolution of poorly water-soluble drugs. International Journal of Pharmaceutics, 312(1-2), 179-186. doi: 10. 1016/j. ijpharm. 2006. 01. 008.
-
(2006)
International Journal of Pharmaceutics
, vol.312
, Issue.1-2
, pp. 179-186
-
-
Kocbek, P.1
Baumgartner, S.2
Kristl, J.3
-
41
-
-
0035292910
-
Influence of physicochemical propertieson dissolution of drugs in the gastrointestinal tract
-
doi:10.1016/S0169-409X(00)00130-7
-
Horter, D., & Dressman, J. B. (2001). Influence of physicochemical propertieson dissolution of drugs in the gastrointestinal tract. Advanced Drug Delivery Reviews, 46(1-3), 75-87. doi: 10. 1016/S0169-409X(00)00130-7.
-
(2001)
Advanced Drug Delivery Reviews
, vol.46
, Issue.1-3
, pp. 75-87
-
-
Horter, D.1
Dressman, J.B.2
-
42
-
-
77952488307
-
Emerging nanotechnology approaches for HIV/AIDS treatment and prevention
-
doi:10.2217/nnm.10.1
-
Mamo, T., Moseman, E. A., Kolishetti, N., Salvador-Morales, C., et al. (2010). Emerging nanotechnology approaches for HIV/AIDS treatment and prevention. Nanomedicine, 5(2), 269-285. doi: 10. 2217/nnm. 10. 1.
-
(2010)
Nanomedicine
, vol.5
, Issue.2
, pp. 269-285
-
-
Mamo, T.1
Moseman, E.A.2
Kolishetti, N.3
Salvador-Morales, C.4
-
43
-
-
84868685209
-
Biodegradable nanosized particles to deliver sustained-release medication cargo. Nanomedicine: nanomateral
-
Published online: Azonano.com; The A to Z of nanotechnology
-
Hanel, J. (2010). Biodegradable nanosized particles to deliver sustained-release medication cargo. Nanomedicine: nanomateral. PNAS, 2009(106), 19268-19273. Published online: Azonano. com; The A to Z of nanotechnology.
-
(2010)
Pnas
, vol.2009
, Issue.106
, pp. 19268-19273
-
-
Hanel, J.1
-
44
-
-
84878021337
-
Nanotechnology-based cancer treatment can reduce side effects
-
Published online. Available at Last accessed on 25 Jun 2012
-
Soutter, W. (2012). Nanotechnology-based cancer treatment can reduce side effects. Nanomedicine: nanomateral. Published online. Available at: http://www. azonano. com/news. aspx?newsID=25010. Last accessed on 25 Jun 2012.
-
(2012)
Nanomedicine: Nanomateral
-
-
Soutter, W.1
-
45
-
-
79960605617
-
Lipid-polymer hybrid nanoparticles: synthesis, characterization and application
-
doi:10.1142/S179398441000016X
-
Zhang, L., & Zhang, L. G. (2010). Lipid-polymer hybrid nanoparticles: synthesis, characterization and application. Nano LIFE, 1(1-2), 163-173. doi: 10. 1142/S179398441000016X.
-
(2010)
Nano LIFE
, vol.1
, Issue.1-2
, pp. 163-173
-
-
Zhang, L.1
Zhang, L.G.2
-
46
-
-
82155187080
-
Biodegradable nanoparticles are excellent vehicle for site directed in vivo delivery of drugs and vaccines
-
doi:10.1186/1477-3155-9-55
-
Mahapatro, A., & Singh, D. K. (2011). Biodegradable nanoparticles are excellent vehicle for site directed in vivo delivery of drugs and vaccines. Journal of Nanobiotechnology, 9, 55-67. doi: 10. 1186/1477-3155-9-55.
-
(2011)
Journal of Nanobiotechnology
, vol.9
, pp. 55-67
-
-
Mahapatro, A.1
Singh, D.K.2
-
47
-
-
61349139614
-
Drug delivery and nanoparticles: applications and hazards
-
PMCID: PMC2527668
-
Jong, W. H. D., & Borm, P. J. A. (2008). Drug delivery and nanoparticles: applications and hazards. International Journal of Nanomedicine, 3(1), 133-149 PMCID: PMC2527668.
-
(2008)
International Journal of Nanomedicine
, vol.3
, Issue.1
, pp. 133-149
-
-
Jong, W.H.D.1
Borm, P.J.A.2
-
48
-
-
35248864881
-
Nanoparticles in drug delivery and environmental exposure: same size, same risk?
-
doi:10.2217/17435889.1.2.235
-
BormPJ, M.-S. D. (2006). Nanoparticles in drug delivery and environmental exposure: same size, same risk? Nanomedicine, 1(2), 235-249. doi: 10. 2217/17435889. 1. 2. 235.
-
(2006)
Nanomedicine
, vol.1
, Issue.2
, pp. 235-249
-
-
Bormpj, M.-S.D.1
-
49
-
-
0031568939
-
Nanoparticle drug delivery system forrestenosis
-
doi:10.1016/S0169-409X(96)00483-8
-
Labhasetwar, V., Song, C., Levy, R. J. (1997). Nanoparticle drug delivery system forrestenosis. Advanced Drug Delivery Reviews, 24(1), 63-85. doi: 10. 1016/S0169-409X(96)00483-8.
-
(1997)
Advanced Drug Delivery Reviews
, vol.24
, Issue.1
, pp. 63-85
-
-
Labhasetwar, V.1
Song, C.2
Levy, R.J.3
-
50
-
-
0033956526
-
Biomaterials in drug delivery and tissue engineering: one laboratory's experience
-
doi:10.1021/ar9800993
-
Langer, R. (2000). Biomaterials in drug delivery and tissue engineering: one laboratory's experience. Accounts of Chemical Research, 33(2), 94-101. doi: 10. 1021/ar9800993.
-
(2000)
Accounts of Chemical Research
, vol.33
, Issue.2
, pp. 94-101
-
-
Langer, R.1
-
51
-
-
0037433811
-
A PEGylated dendritic nanoparticulate carrier of fluorouracil
-
doi:10.1016/S0378-5173(03)00132-7
-
Bhadra, D., Bhadra, S., Jain, P., Jain, N. K. (2003). A PEGylated dendritic nanoparticulate carrier of fluorouracil. International Journal of Pharmaceutics, 257(1-2), 111-124. doi: 10. 1016/S0378-5173(03)00132-7.
-
(2003)
International Journal of Pharmaceutics
, vol.257
, Issue.1-2
, pp. 111-124
-
-
Bhadra, D.1
Bhadra, S.2
Jain, P.3
Jain, N.K.4
-
52
-
-
30544446478
-
Long-circulating polymeric nanovectors for tumor-selective gene delivery
-
Kommareddy, S., Tiwari, S. B., Amiji, M. M. (2005). Long-circulating polymeric nanovectors for tumor-selective gene delivery. Technology in Cancer Research & Treatment, 4(6), 615-625.
-
(2005)
Technology in Cancer Research & Treatment
, vol.4
, Issue.6
, pp. 615-625
-
-
Kommareddy, S.1
Tiwari, S.B.2
Amiji, M.M.3
-
53
-
-
0036707316
-
Biodegradable nanoparticles for drug delivery and targeting
-
doi:10.1016/S1359-0286(02)00117-1
-
Hans, M. L., & Lowman, A. M. (2002). Biodegradable nanoparticles for drug delivery and targeting. Current Opinion in Solid State and Materials Science, 6(4), 319-327. doi: 10. 1016/S1359-0286(02)00117-1.
-
(2002)
Current Opinion in Solid State and Materials Science
, vol.6
, Issue.4
, pp. 319-327
-
-
Hans, M.L.1
Lowman, A.M.2
-
54
-
-
80052278049
-
Chitosan and its derivatives for drug delivery perspective
-
doi:10.1007/12_2011_117
-
Sonia, T. A., & Sharma, C. P. (2011). Chitosan and its derivatives for drug delivery perspective. Advances in Polymer Science, 243, 23-54. doi: 10. 1007/12_2011_117.
-
(2011)
Advances in Polymer Science
, vol.243
, pp. 23-54
-
-
Sonia, T.A.1
Sharma, C.P.2
-
55
-
-
10844221391
-
Oral evaluation in rabbits of cyclosporin-loaded Eudragit RS or RL nanoparticles
-
doi:10.1016/j.ijpharm.2004.09.019
-
Ubrich, N., Schmidt, C., Bodmeier, R., Hoffman, M., Maincent, P. (2005). Oral evaluation in rabbits of cyclosporin-loaded Eudragit RS or RL nanoparticles. International Journal of Pharmaceutics, 288(1), 169-175. doi: 10. 1016/j. ijpharm. 2004. 09. 019.
-
(2005)
International Journal of Pharmaceutics
, vol.288
, Issue.1
, pp. 169-175
-
-
Ubrich, N.1
Schmidt, C.2
Bodmeier, R.3
Hoffman, M.4
Maincent, P.5
-
56
-
-
0031783879
-
Chitosan and its use as a pharmaceutical excipient
-
doi:10.1023/A:1011929016601
-
Illum, L. (1998). Chitosan and its use as a pharmaceutical excipient. Pharmaceutical Research, 15, 1326-1331. doi: 10. 1023/A: 1011929016601.
-
(1998)
Pharmaceutical Research
, vol.15
, pp. 1326-1331
-
-
Illum, L.1
-
57
-
-
0000812919
-
Nanoparticles
-
J. Kreuter (Ed.), New York: Marcel Dekker
-
Kreuter, J. (1994). Nanoparticles. In J. Kreuter (Ed.), Colloidal drug delivery systems (pp. 261-276). New York: Marcel Dekker.
-
(1994)
Colloidal Drug Delivery Systems
, pp. 261-276
-
-
Kreuter, J.1
-
59
-
-
7444268954
-
Recent advances on chitosan-based micro- and nanoparticles in drug delivery
-
doi:10.1016/j.jconrel.2004.08.010
-
Agnihotri, S. A., Mallikarjuna, N. N., Aminabhavi, T. M. (2004). Recent advances on chitosan-based micro- and nanoparticles in drug delivery. Journal of Controlled Release, 100(1), 5-28. doi: 10. 1016/j. jconrel. 2004. 08. 010.
-
(2004)
Journal of Controlled Release
, vol.100
, Issue.1
, pp. 5-28
-
-
Agnihotri, S.A.1
Mallikarjuna, N.N.2
Aminabhavi, T.M.3
-
60
-
-
11244281032
-
Chitosan-based particles as controlled drug delivery systems
-
doi:10.1080/10717540590889781
-
Prabaharan, M., & Mano, J. F. (2005). Chitosan-based particles as controlled drug delivery systems. Drug Delivery, 12(1), 41-57. doi: 10. 1080/10717540590889781.
-
(2005)
Drug Delivery
, vol.12
, Issue.1
, pp. 41-57
-
-
Prabaharan, M.1
Mano, J.F.2
-
61
-
-
0031004232
-
Chitosan as a nasal delivery system: the effect of chitosan solutions on in vitro and in vivo mucociliary transport rates in human turbinates and volunteers
-
doi:10.1021/js960182o
-
Aspden, T. J., Mason, J. D., Jones, N. S. (1997). Chitosan as a nasal delivery system: the effect of chitosan solutions on in vitro and in vivo mucociliary transport rates in human turbinates and volunteers. Journal of Pharmaceutical Sciences, 86(4), 509-513. doi: 10. 1021/js960182o.
-
(1997)
Journal of Pharmaceutical Sciences
, vol.86
, Issue.4
, pp. 509-513
-
-
Aspden, T.J.1
Mason, J.D.2
Jones, N.S.3
-
62
-
-
0035936972
-
Chitosan-DNA nanoparticles as gene carriers: synthesis, characterization and transfection efficiency
-
doi:10.1016/S0168-3659(00)00361-8
-
Mao, H. Q., Troung-le, V. L., Janes, K. A., Roy, K., Wang, Y., August, J. T., Leong, K. W. (2001). Chitosan-DNA nanoparticles as gene carriers: synthesis, characterization and transfection efficiency. Journal of Controlled Release, 70(3), 399-421. doi: 10. 1016/S0168-3659(00)00361-8.
-
(2001)
Journal of Controlled Release
, vol.70
, Issue.3
, pp. 399-421
-
-
Mao, H.Q.1
Troung-Le, V.L.2
Janes, K.A.3
Roy, K.4
Wang, Y.5
August, J.T.6
Leong, K.W.7
-
63
-
-
54949153043
-
Preparation of estradiol chitosan nanoparticles for improving nasal absorption and brain targeting
-
doi:10.1016/j.ejpb.2008.07.005
-
Wang, X., Chi, N., Tang, X. (2008). Preparation of estradiol chitosan nanoparticles for improving nasal absorption and brain targeting. European Journal of Pharmaceutics and Biopharmaceutics, 70(3), 735-740. doi: 10. 1016/j. ejpb. 2008. 07. 005.
-
(2008)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.70
, Issue.3
, pp. 735-740
-
-
Wang, X.1
Chi, N.2
Tang, X.3
-
64
-
-
0031550212
-
Novel hydrophilic chitosan-polyethylene oxide nanoparticles as protein carriers
-
doi:0021-8995/97/010125-08
-
Calvo, et al. (1997). Novel hydrophilic chitosan-polyethylene oxide nanoparticles as protein carriers. Journal of Applied Polymer Science, 63, 125-132. doi: 0021-8995/97/010125-08.
-
(1997)
Journal of Applied Polymer Science
, vol.63
, pp. 125-132
-
-
Calvo1
-
65
-
-
0024371139
-
A novel approach to the oral delivery of micro- or nanoparticles
-
doi:10.1023/A:1015987516796
-
Bodmeier, R., Chen, H. G., Paeratakul, O. (1989). A novel approach to the oral delivery of micro- or nanoparticles. Pharmaceutical Research, 6(5), 413-417. doi: 10. 1023/A: 1015987516796.
-
(1989)
Pharmaceutical Research
, vol.6
, Issue.5
, pp. 413-417
-
-
Bodmeier, R.1
Chen, H.G.2
Paeratakul, O.3
-
66
-
-
0037027876
-
Bioadhesive polysaccharide in protein delivery system: chitosan nanoparticles improve the intestinal absorption of insulin in vivo
-
doi:10.1016/S0378-5173(02)00486-6
-
Pan, Y., Li, Y. J., Zhao, H. Y., Zheng, J. M., Xu, H., Wei, G., Hao, J. S., Cui, F. D. (2002). Bioadhesive polysaccharide in protein delivery system: chitosan nanoparticles improve the intestinal absorption of insulin in vivo. International Journal of Pharmaceutics, 249(1-2), 139-147. doi: 10. 1016/S0378-5173(02)00486-6.
-
(2002)
International Journal of Pharmaceutics
, vol.249
, Issue.1-2
, pp. 139-147
-
-
Pan, Y.1
Li, Y.J.2
Zhao, H.Y.3
Zheng, J.M.4
Xu, H.5
Wei, G.6
Hao, J.S.7
Cui, F.D.8
-
67
-
-
84859077437
-
Preparation and in vitro characterization of chitosan nanoparticles containing Mesobuthus eupeus scorpion venom as an antigen delivery system
-
doi:10.1590/S1678-91992012000100006
-
Dustgani, A., Fasahani, E. V., Imani, M. (2012). Preparation and in vitro characterization of chitosan nanoparticles containing Mesobuthus eupeus scorpion venom as an antigen delivery system. Journal of Venomous Animals and Toxins including Tropical Diseases, 18(1), 44-52. doi: 10. 1590/S1678-91992012000100006.
-
(2012)
Journal of Venomous Animals and Toxins including Tropical Diseases
, vol.18
, Issue.1
, pp. 44-52
-
-
Dustgani, A.1
Fasahani, E.V.2
Imani, M.3
-
68
-
-
67650809319
-
Adsorption of nuclease p1 on chitosan nano-particles
-
doi:10.1590/S0104-66322009000200022
-
Shi, L. E., & Tang, Z. X. (2007). Adsorption of nuclease p1 on chitosan nano-particles. Brazilian Journal of Chemical Engineering, 26(2), 223-228. doi: 10. 1590/S0104-66322009000200022.
-
(2007)
Brazilian Journal of Chemical Engineering
, vol.26
, Issue.2
, pp. 223-228
-
-
Shi, L.E.1
Tang, Z.X.2
-
69
-
-
23444441931
-
Modulation of surface charge, particle size and morphological properties of chitosan-TPP nanoparticles intended for gene delivery
-
doi:10.1016/j.colsurfb.2005.06.001
-
Gan, Q., Wang, T., Cochrane, C., McCarron, P. (2005). Modulation of surface charge, particle size and morphological properties of chitosan-TPP nanoparticles intended for gene delivery. Colloids and Surfaces B, 44(2-3), 65-73. doi: 10. 1016/j. colsurfb. 2005. 06. 001.
-
(2005)
Colloids and Surfaces B
, vol.44
, Issue.2-3
, pp. 65-73
-
-
Gan, Q.1
Wang, T.2
Cochrane, C.3
McCarron, P.4
-
70
-
-
36549048398
-
Cavitation effects versus stretch effects resulted in different size and polydispersity of ionotropic gelation chitosan-sodium tripolyphosphate nanoparticle
-
Tsai, M. L., Bai, S. W., Chen, R. H. (2008). Cavitation effects versus stretch effects resulted in different size and polydispersity of ionotropic gelation chitosan-sodium tripolyphosphate nanoparticle. Carbohydrate Polymers, 71(3), 448-457.
-
(2008)
Carbohydrate Polymers
, vol.71
, Issue.3
, pp. 448-457
-
-
Tsai, M.L.1
Bai, S.W.2
Chen, R.H.3
-
71
-
-
13844272505
-
Physicochemical characterization of chitosan nanoparticles: electrokinetic and stability behavior
-
doi:10.1016/j.jcis.2004.08.186
-
López-León, T., Carvalho, E. L., Seijo, B., Ortega-Vinuesa, J. L., Bastos-González, D. (2005). Physicochemical characterization of chitosan nanoparticles: electrokinetic and stability behavior. Journal of Colloid and Interface Science, 283(2), 344-351. doi: 10. 1016/j. jcis. 2004. 08. 186.
-
(2005)
Journal of Colloid and Interface Science
, vol.283
, Issue.2
, pp. 344-351
-
-
López-León, T.1
Carvalho, E.L.2
Seijo, B.3
Ortega-Vinuesa, J.L.4
Bastos-González, D.5
-
72
-
-
35848959714
-
Alginate/chitosan nanoparticles are effective for oral insulin delivery
-
doi:10.1007/s11095-007-9367-4
-
Sarmento, B., Ribeiro, A. J., Veiga, F., Ferreira, D. (2007). Alginate/chitosan nanoparticles are effective for oral insulin delivery. Pharmaceutical Research, 24(12), 2198-2206. doi: 10. 1007/s11095-007-9367-4.
-
(2007)
Pharmaceutical Research
, vol.24
, Issue.12
, pp. 2198-2206
-
-
Sarmento, B.1
Ribeiro, A.J.2
Veiga, F.3
Ferreira, D.4
-
73
-
-
0346094226
-
Low molecular weight chitosan nanoparticles as new carriers for nasal vaccine delivery in mice
-
doi:10.1016/j.ejpb.2003.09.006
-
Vila, A., Sánchez, A., Janes, K., Behrens, I., Kissel, T., Vila Jato, J. L., Alonso, M. J. (2004). Low molecular weight chitosan nanoparticles as new carriers for nasal vaccine delivery in mice. The European Journal of Pharmaceutical, 57(1), 123-131. doi: 10. 1016/j. ejpb. 2003. 09. 006.
-
(2004)
The European Journal of Pharmaceutical
, vol.57
, Issue.1
, pp. 123-131
-
-
Vila, A.1
Sánchez, A.2
Janes, K.3
Behrens, I.4
Kissel, T.5
Vila Jato, J.L.6
Alonso, M.J.7
-
74
-
-
0141719284
-
Enhancement of nasal absorbtion of insulin using chitosan nanoparticles
-
doi:10.1023/A:1018908705446
-
Fernandez-Urrusuno, R., Calvo, P., Remunan-Lopez, C., Vila-Jato, J. L., Alonso, M. J. (1999). Enhancement of nasal absorbtion of insulin using chitosan nanoparticles. Pharmaceutical Research, 16, 1576-1581. doi: 10. 1023/A: 1018908705446.
-
(1999)
Pharmaceutical Research
, vol.16
, pp. 1576-1581
-
-
Fernandez-Urrusuno, R.1
Calvo, P.2
Remunan-Lopez, C.3
Vila-Jato, J.L.4
Alonso, M.J.5
-
75
-
-
21344446354
-
Preparation and in vitro evaluation of chitosan nanoparticles containing a caspase inhibitor
-
doi:10.1016/j.ijpharm.2005.03.027
-
Aktas, Y., Andrieux, K., Alonso, M. J., Calvo, P., Gürsoy, R. N., Couvreur, P., Capan, Y. (2005). Preparation and in vitro evaluation of chitosan nanoparticles containing a caspase inhibitor. International Journal of Pharmaceutics, 298, 378-383. doi: 10. 1016/j. ijpharm. 2005. 03. 027.
-
(2005)
International Journal of Pharmaceutics
, vol.298
, pp. 378-383
-
-
Aktas, Y.1
Andrieux, K.2
Alonso, M.J.3
Calvo, P.4
Gürsoy, R.N.5
Couvreur, P.6
Capan, Y.7
-
76
-
-
0035859983
-
Chitosan nanoparticles: a new vehicle for the improvement of the delivery of drugs to the ocular surface: application to cyclosporine A
-
doi:10.1016/S0378-5173(01)00760-8
-
DeCampos, A. M., & Alonso, M. J. (2001). Chitosan nanoparticles: a new vehicle for the improvement of the delivery of drugs to the ocular surface: application to cyclosporine A. International Journal of Pharmaceutics, 224(1-2), 116-159. doi: 10. 1016/S0378-5173(01)00760-8.
-
(2001)
International Journal of Pharmaceutics
, vol.224
, Issue.1-2
, pp. 116-159
-
-
Decampos, A.M.1
Alonso, M.J.2
-
77
-
-
0034657513
-
A novel approach to prepare tripolyphosphate/chitosan complex beads for controlled release drug delivery
-
doi:10.1016/S0378-5173(00)00403-8
-
Shu, X. Z., & Zhu, K. J. (2000). A novel approach to prepare tripolyphosphate/chitosan complex beads for controlled release drug delivery. International Journal of Pharmaceutics, 201(1), 51-58. doi: 10. 1016/S0378-5173(00)00403-8.
-
(2000)
International Journal of Pharmaceutics
, vol.201
, Issue.1
, pp. 51-58
-
-
Shu, X.Z.1
Zhu, K.J.2
-
78
-
-
78649908528
-
Formulation and in vitro characterization of Eudragit® L100 and Eudragit® L100-PLGA nanoparticles containing diclofenac sodium
-
doi:10.1208/s12249-010-9489-6
-
Cetin, M., Atila, A., Kadioglu, Y. (2010). Formulation and in vitro characterization of Eudragit® L100 and Eudragit® L100-PLGA nanoparticles containing diclofenac sodium. AAPS PharmSciTech, 11(3), 1250-1256. doi: 10. 1208/s12249-010-9489-6.
-
(2010)
AAPS PharmSciTech
, vol.11
, Issue.3
, pp. 1250-1256
-
-
Cetin, M.1
Atila, A.2
Kadioglu, Y.3
-
79
-
-
75149163234
-
Preparation and characterization of insulin nanoparticles using chitosan and Arabic gum with ionic gelation method
-
doi:10.1016/j.nano.2009.04.007
-
Avadi, M. R., Sadeghi, A. M. M., Mohammadpour, N., et al. (2010). Preparation and characterization of insulin nanoparticles using chitosan and Arabic gum with ionic gelation method. Nanomedicine: Nanotechnology, Biology and Medicine, 6(1), 58-63. doi: 10. 1016/j. nano. 2009. 04. 007.
-
(2010)
Nanomedicine: Nanotechnology, Biology and Medicine
, vol.6
, Issue.1
, pp. 58-63
-
-
Avadi, M.R.1
Sadeghi, A.M.M.2
Mohammadpour, N.3
-
80
-
-
70450223491
-
-
US patent 5, 874 111
-
Maitra, A. N., Ghosh, P. K., De, T. K., Sahoo, S. K. (1999) Process for the preparation of highly monodispersed hydrophilic polymeric nanoparticles of size less than 100 nm. US patent 5, 874, 111.
-
(1999)
Process for the preparation of highly monodispersed hydrophilic polymeric nanoparticles of size less than 100 nm
-
-
Maitra, A.N.1
Ghosh, P.K.2
De, T.K.3
Sahoo, S.K.4
-
81
-
-
0027468519
-
Release behavior of 5-fluorouracil from chitosan-gel nanospheres immobilizing 5-fluorouracil coated with polysaccharides and their cell specific cytotoxicity
-
doi:10.3109/02652049309015307
-
Ohya, Y., Shiratani, M., Kobayashi, H., Ouchi, T. (1993). Release behavior of 5-fluorouracil from chitosan-gel nanospheres immobilizing 5-fluorouracil coated with polysaccharides and their cell specific cytotoxicity. Journal of Microencapsulation, 10(1), 1-9. doi: 10. 3109/02652049309015307.
-
(1993)
Journal of Microencapsulation
, vol.10
, Issue.1
, pp. 1-9
-
-
Ohya, Y.1
Shiratani, M.2
Kobayashi, H.3
Ouchi, T.4
-
82
-
-
33947150969
-
Nanostructured materials for applications in drug delivery and tissue engineering
-
doi:10.1163/156856207779996931
-
Goldberg, M., Langer, R., Jia, X. (2007). Nanostructured materials for applications in drug delivery and tissue engineering. Journal of Biomaterials Science, Polymer Edition, 18(3), 241-268. doi: 10. 1163/156856207779996931.
-
(2007)
Journal of Biomaterials Science, Polymer Edition
, vol.18
, Issue.3
, pp. 241-268
-
-
Goldberg, M.1
Langer, R.2
Jia, X.3
-
83
-
-
0035816156
-
Tumour targeted delivery of encapsulated dextran-doxorubicin conjugate using chitosan nanoparticles as carrier
-
doi:10.1016/S0168-3659(01)00342-X
-
Mitra, S., Gaur, U., Ghosh, P. C., Maitra, A. N. (2001). Tumour targeted delivery of encapsulated dextran-doxorubicin conjugate using chitosan nanoparticles as carrier. Journal of Controlled Release, 74(1-3), 317-323. doi: 10. 1016/S0168-3659(01)00342-X.
-
(2001)
Journal of Controlled Release
, vol.74
, Issue.1-3
, pp. 317-323
-
-
Mitra, S.1
Gaur, U.2
Ghosh, P.C.3
Maitra, A.N.4
-
84
-
-
77955525250
-
4-chitosan nanoparticles used for hyperthermia
-
doi:10.1016/j.apt.2010.01.008
-
4-chitosan nanoparticles used for hyperthermia. Advanced Powder Technology, 21(4), 461-467. doi: 10. 1016/j. apt. 2010. 01. 008.
-
(2010)
Advanced Powder Technology
, vol.21
, Issue.4
, pp. 461-467
-
-
Qu, J.1
Liu, G.2
Wang, Y.3
Hong, R.4
-
85
-
-
0032127562
-
Chitosan-chondroitin sulfate and chitosan-hyaluronate polyelectrolyte complexes: biological properties
-
doi:10.1016/S0142-9612(98)00036-2
-
Denuziere, A., Ferrier, D., Damour, O., Domard, A. (1998). Chitosan-chondroitin sulfate and chitosan-hyaluronate polyelectrolyte complexes: biological properties. Biomaterials, 19(14), 1275-1285. doi: 10. 1016/S0142-9612(98)00036-2.
-
(1998)
Biomaterials
, vol.19
, Issue.14
, pp. 1275-1285
-
-
Denuziere, A.1
Ferrier, D.2
Damour, O.3
Domard, A.4
-
86
-
-
15044341172
-
Chitosan-dextran sulfate nanoparticles for delivery of an anti-angiogenesis peptide
-
doi:10.1007/s10989-004-2433-4
-
Chen, Y., Mohanraj, V. J., Parkin, J. E. (2003). Chitosan-dextran sulfate nanoparticles for delivery of an anti-angiogenesis peptide. International Journal of Peptide Research and Therapeutics, 10(5-6), 621-629. doi: 10. 1007/s10989-004-2433-4.
-
(2003)
International Journal of Peptide Research and Therapeutics
, vol.10
, Issue.5-6
, pp. 621-629
-
-
Chen, Y.1
Mohanraj, V.J.2
Parkin, J.E.3
-
87
-
-
37249075464
-
Designing chitosan-dextran sulfate nanoparticles using charge ratios
-
doi:10.1208/pt0804098
-
Chen, Y., Mohanraj, V. J., Wang, F., Benson, H. A. E. (2007). Designing chitosan-dextran sulfate nanoparticles using charge ratios. AAPS PharmSciTech, 8(4), 131-139. doi: 10. 1208/pt0804098.
-
(2007)
AAPS PharmSciTech
, vol.8
, Issue.4
, pp. 131-139
-
-
Chen, Y.1
Mohanraj, V.J.2
Wang, F.3
Benson, H.A.E.4
-
88
-
-
25844462278
-
Formation of biocompatible nanoparticles by self-assembly of enzymatic hydrolysates of chitosan and carboxymethyl cellulose
-
doi:10.1271/bbb.69.1637
-
Ichikawa, S., Iwamoto, S., Watanabe, J. (2005). Formation of biocompatible nanoparticles by self-assembly of enzymatic hydrolysates of chitosan and carboxymethyl cellulose. Bioscience, Biotechnology, and Biochemistry, 69(9), 1637-1642. doi: 10. 1271/bbb. 69. 1637.
-
(2005)
Bioscience, Biotechnology, and Biochemistry
, vol.69
, Issue.9
, pp. 1637-1642
-
-
Ichikawa, S.1
Iwamoto, S.2
Watanabe, J.3
-
89
-
-
36048937633
-
Heparin/chitosan nanoparticle carriers prepared by polyelectrolyte complexation
-
doi:10.1002/jbm.a.31407
-
Liu, Z., Jiao, Y., Liu, F., Zhang, Z. (2007). Heparin/chitosan nanoparticle carriers prepared by polyelectrolyte complexation. Journal of Biomedical Materials Research Part A, 83(3), 806-812. doi: 10. 1002/jbm. a. 31407.
-
(2007)
Journal of Biomedical Materials Research Part A
, vol.83
, Issue.3
, pp. 806-812
-
-
Liu, Z.1
Jiao, Y.2
Liu, F.3
Zhang, Z.4
-
90
-
-
80155194439
-
Controlled release of chitosan/heparin nanoparticle-delivered VEGF enhances regeneration of decellularized tissue-engineered scaffolds
-
doi:10.2147/IJN.S18753
-
Tan, Q., Tang, H., Hu, J., Hu, Y., Zhou, X., Tao, Y., Wu, Z. (2011). Controlled release of chitosan/heparin nanoparticle-delivered VEGF enhances regeneration of decellularized tissue-engineered scaffolds. International Journal of Nanomedicine, 6, 929-942. doi: 10. 2147/IJN. S18753.
-
(2011)
International Journal of Nanomedicine
, vol.6
, pp. 929-942
-
-
Tan, Q.1
Tang, H.2
Hu, J.3
Hu, Y.4
Zhou, X.5
Tao, Y.6
Wu, Z.7
-
91
-
-
33845566719
-
Formulation and characterization of amphotericin B-chitosan-dextran sulfate nanoparticles
-
doi:10.1016/j.ijpharm.2006.08.013
-
Tiyaboonchai, W., & Limpeanchob, N. (2007). Formulation and characterization of amphotericin B-chitosan-dextran sulfate nanoparticles. International Journal of Pharmaceutics, 329(1-2), 142-149. doi: 10. 1016/j. ijpharm. 2006. 08. 013.
-
(2007)
International Journal of Pharmaceutics
, vol.329
, Issue.1-2
, pp. 142-149
-
-
Tiyaboonchai, W.1
Limpeanchob, N.2
-
92
-
-
0031722107
-
Chitosan-based vector/DNA complexes for gene delivery: biophysical characteristics and transfection ability
-
doi:10.1023/A:1011981000671
-
Erbacher, P., Zou, S., Bettinger, T., Steffan, A. M., Remy, J. S. (1998). Chitosan-based vector/DNA complexes for gene delivery: biophysical characteristics and transfection ability. Pharmaceutical Research, 15(9), 1332-1339. doi: 10. 1023/A: 1011981000671.
-
(1998)
Pharmaceutical Research
, vol.15
, Issue.9
, pp. 1332-1339
-
-
Erbacher, P.1
Zou, S.2
Bettinger, T.3
Steffan, A.M.4
Remy, J.S.5
-
93
-
-
33745094433
-
Development and comparison of different nanoparticulate polyelectrolyte complexes as insulin carriers
-
doi:10.1007/s10989-005-9010-3
-
Sarmento, B., Martins, S., Ribeiro, A., Veiga, F., Neufeld, R., Ferreira, D. (2006). Development and comparison of different nanoparticulate polyelectrolyte complexes as insulin carriers. The International Journal of Peptide Research and Therapeutics, 12(2), 131-138. doi: 10. 1007/s10989-005-9010-3.
-
(2006)
The International Journal of Peptide Research and Therapeutics
, vol.12
, Issue.2
, pp. 131-138
-
-
Sarmento, B.1
Martins, S.2
Ribeiro, A.3
Veiga, F.4
Neufeld, R.5
Ferreira, D.6
-
94
-
-
50249129610
-
Permeation enhancer effect of chitosan and chitosan derivatives: comparison of formulations as soluble polymers and nanoparticulate systems on insulin absorption in Caco-2 cells
-
doi:10.1016/j.ejpb.2008.03.004
-
Sadeghi, A. M., Dorkoosh, F. A., Avadi, M. R., Weinhold, M., et al. (2008). Permeation enhancer effect of chitosan and chitosan derivatives: comparison of formulations as soluble polymers and nanoparticulate systems on insulin absorption in Caco-2 cells. European Journal of Pharmaceutics and Biopharmaceutics, 70(1), 270-278. doi: 10. 1016/j. ejpb. 2008. 03. 004.
-
(2008)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.70
, Issue.1
, pp. 270-278
-
-
Sadeghi, A.M.1
Dorkoosh, F.A.2
Avadi, M.R.3
Weinhold, M.4
-
95
-
-
0034952922
-
Chitosan-alginate microparticles as a protein carrier
-
doi:10.1081/DDC-100104314
-
Coppi, G., Iannuccelli, V., Leo, E., Bernabei, M. T., Cameroni, R. (2001). Chitosan-alginate microparticles as a protein carrier. Drug Development and Industrial Pharmacy, 27(5), 393-400. doi: 10. 1081/DDC-100104314.
-
(2001)
Drug Development and Industrial Pharmacy
, vol.27
, Issue.5
, pp. 393-400
-
-
Coppi, G.1
Iannuccelli, V.2
Leo, E.3
Bernabei, M.T.4
Cameroni, R.5
-
96
-
-
23844472633
-
Effect of experimental parameters on the formation of alginate-chitosan nanoparticles and evaluation of their potential application as DNA carrier
-
doi:10.1163/1568562052843339
-
Douglas, K. L., & Tabrizian, M. (2005). Effect of experimental parameters on the formation of alginate-chitosan nanoparticles and evaluation of their potential application as DNA carrier. Journal of Biomaterials Science, 16(1), 43-56. doi: 10. 1163/1568562052843339.
-
(2005)
Journal of Biomaterials Science
, vol.16
, Issue.1
, pp. 43-56
-
-
Douglas, K.L.1
Tabrizian, M.2
-
97
-
-
33748631285
-
Characterization of insulin-loaded alginate nanoparticles produced by ionotropic pre-gelation through DSC and FTIR studies
-
doi:10.1016/j.carbpol.2006.02.008
-
Sarmento, B., Ferreira, D., Veiga, F., Ribeiro, A. (2006). Characterization of insulin-loaded alginate nanoparticles produced by ionotropic pre-gelation through DSC and FTIR studies. Carbohydrate Polymers, 66, 1-7. doi: 10. 1016/j. carbpol. 2006. 02. 008.
-
(2006)
Carbohydrate Polymers
, vol.66
, pp. 1-7
-
-
Sarmento, B.1
Ferreira, D.2
Veiga, F.3
Ribeiro, A.4
-
98
-
-
35348895676
-
Nanoparticles based on the complex of chitosan and polyaspartic acid sodium salt: preparation, characterization and the use for 5-fluorouracil delivery
-
doi:10.1016/j.ejpb.2007.04.007
-
Zhang, Y., Yang, W., Wang, C., Hu, J., Fu, S., Dong, L., Wu, L., Shen, X. (2007). Nanoparticles based on the complex of chitosan and polyaspartic acid sodium salt: preparation, characterization and the use for 5-fluorouracil delivery. European Journal of Pharmaceutics and Biopharmaceutics, 67, 621-631. doi: 10. 1016/j. ejpb. 2007. 04. 007.
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.67
, pp. 621-631
-
-
Zhang, Y.1
Yang, W.2
Wang, C.3
Hu, J.4
Fu, S.5
Dong, L.6
Wu, L.7
Shen, X.8
-
99
-
-
54349097782
-
Preparation of chitosan-polyaspartic acid-5-fluorouracil nanoparticles and its anti-carcinoma effect on tumor growth in nude mice
-
doi:10.3748/wjg.14.3554
-
Zhang, D. Y., Shen, X. Z., Wang, J. Y., Dong, L., Zheng, Y. L., Wu, L. L. (2008). Preparation of chitosan-polyaspartic acid-5-fluorouracil nanoparticles and its anti-carcinoma effect on tumor growth in nude mice. World Journal of Gastroenterology, 14, 3554-3562. doi: 10. 3748/wjg. 14. 3554.
-
(2008)
World Journal of Gastroenterology
, vol.14
, pp. 3554-3562
-
-
Zhang, D.Y.1
Shen, X.Z.2
Wang, J.Y.3
Dong, L.4
Zheng, Y.L.5
Wu, L.L.6
-
100
-
-
84878021154
-
-
Available online Accessed: 23 Jun 2012
-
Lee, J. E., Khan, S. A., Lim, K. H. Chitosan-nanoparticle preparationby polyelectrolyte complexation. 1-2. Available online: http://wjoe. hebeu. edu. cn/ICCE-17%20proceedings%20Hawaii%20USA/Lee,%20Eun-Ju%20%28Kyungpook%20Nat. U.,%20Daegu,%20Korea%29%20%20541. pdf. Accessed: 23 Jun 2012.
-
Chitosan-nanoparticle preparationby polyelectrolyte complexation. 1-2
-
-
Lee, J.E.1
Khan, S.A.2
Lim, K.H.3
-
101
-
-
0033295619
-
Searching for alternatives to heparin: sulfated fucans from marine invertebrates
-
doi:10.1016/S1050-1738(00)00032-3
-
Mourao, P. A. S., & Pereira, M. S. (1999). Searching for alternatives to heparin: sulfated fucans from marine invertebrates. Trends in Cardiovascular Medicine, 9, 225-232. doi: 10. 1016/S1050-1738(00)00032-3.
-
(1999)
Trends in Cardiovascular Medicine
, vol.9
, pp. 225-232
-
-
Mourao, P.A.S.1
Pereira, M.S.2
-
102
-
-
0032661368
-
Chitosan-polyelectrolyte complexation for the preparation of gel beads and controlled release of anticancer drug. II. Effect of pH-dependent ionic crosslinking or interpolymer complex using tripolyphosphate or polyphosphate as reagent
-
doi:10.1002/(SICI)1097-4628(19991114)74:7<1868::AID-APP32>3.0.CO;2-N
-
Mi, F. L., Shyu, S. S., Kuan, C. Y., Lee, S. L., Lu, K. T., Jang, S. F. (1999). Chitosan-polyelectrolyte complexation for the preparation of gel beads and controlled release of anticancer drug. II. Effect of pH-dependent ionic crosslinking or interpolymer complex using tripolyphosphate or polyphosphate as reagent. Journal of Applied Polymer Science, 74, 1093-1107. doi: 10. 1002/(SICI)1097-4628(19991114)74: 7< 1868:: AID-APP32> 3. 0. CO; 2-N.
-
(1999)
Journal of Applied Polymer Science
, vol.74
, pp. 1093-1107
-
-
Mi, F.L.1
Shyu, S.S.2
Kuan, C.Y.3
Lee, S.L.4
Lu, K.T.5
Jang, S.F.6
-
103
-
-
0034879035
-
Chitosan: some pharmaceutical and biological aspects-an update
-
doi:10.1211/0022357011776441
-
Singla, A. K., & Chawla, M. (2001). Chitosan: some pharmaceutical and biological aspects-an update. The Journal of Pharmacy and Pharmacology, 53(8), 1047-1067. doi: 10. 1211/0022357011776441.
-
(2001)
The Journal of Pharmacy and Pharmacology
, vol.53
, Issue.8
, pp. 1047-1067
-
-
Singla, A.K.1
Chawla, M.2
-
104
-
-
0346724867
-
Comparative studies on polyelectrolyte complexes and mixtures of chitosan-alginate and chitosan-carrageenan as prolonged diltiazemclorhydrate release systems
-
doi:10.1016/S0939-6411(03)00153-X
-
Tapia, C., Escobar, Z., Costa, E., Sapag-Hagar, J., Valenzuela, F., Basualto, C., Nella, G. M., Yazdano-Pedram, M. (2004). Comparative studies on polyelectrolyte complexes and mixtures of chitosan-alginate and chitosan-carrageenan as prolonged diltiazemclorhydrate release systems. European Journal of Pharmaceutics and Biopharmaceutics, 57(1), 65-75. doi: 10. 1016/S0939-6411(03)00153-X.
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 65-75
-
-
Tapia, C.1
Escobar, Z.2
Costa, E.3
Sapag-Hagar, J.4
Valenzuela, F.5
Basualto, C.6
Nella, G.M.7
Yazdano-Pedram, M.8
-
105
-
-
0346094226
-
Low molecular weight chitosan nanoparticles as new carriers for nasal vaccine delivery in mice
-
doi:10.1016/j.ejpb.2003.09.006
-
Vila, A., Sanchez, A., Janes, K., Behrens, I., Kissel, T., Vila-Jato, J. L., Alonso, M. J. (2004). Low molecular weight chitosan nanoparticles as new carriers for nasal vaccine delivery in mice. European Journal of Pharmaceutics and Biopharmaceutics, 57(1), 123-131. doi: 10. 1016/j. ejpb. 2003. 09. 006.
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 123-131
-
-
Vila, A.1
Sanchez, A.2
Janes, K.3
Behrens, I.4
Kissel, T.5
Vila-Jato, J.L.6
Alonso, M.J.7
-
106
-
-
0035813684
-
Chitosan for gene delivery
-
doi:10.1016/S0169-409X(01)00198-3
-
Borchard, G. (2001). Chitosan for gene delivery. Advanced Drug Delivery Reviews, 52(2), 145-150. doi: 10. 1016/S0169-409X(01)00198-3.
-
(2001)
Advanced Drug Delivery Reviews
, vol.52
, Issue.2
, pp. 145-150
-
-
Borchard, G.1
-
107
-
-
0036027454
-
Quaternized chitosan oligomers as novel gene delivery vectors in epithelial cell lines
-
doi:10.1016/S0142-9612(01)00090-4
-
Thanou, M., Florea, B., Geldof, M., Junginger, H. E., Borchard, G. (2002). Quaternized chitosan oligomers as novel gene delivery vectors in epithelial cell lines. Biomaterials, 23(1), 153-159. doi: 10. 1016/S0142-9612(01)00090-4.
-
(2002)
Biomaterials
, vol.23
, Issue.1
, pp. 153-159
-
-
Thanou, M.1
Florea, B.2
Geldof, M.3
Junginger, H.E.4
Borchard, G.5
-
108
-
-
1642346980
-
Long-term expressionwith a cationic polymer derived from a natural polysaccharide: schizophyllan
-
doi:10.1021/bc034178x
-
Nagasaki, T., Hojo, M., Uno, A., Satch, T., Koumoto, K., Mizu, M., Sakurai, K., Shinkai, S. (2004). Long-term expressionwith a cationic polymer derived from a natural polysaccharide: schizophyllan. Bioconjugate Chemistry, 15(2), 249-259. doi: 10. 1021/bc034178x.
-
(2004)
Bioconjugate Chemistry
, vol.15
, Issue.2
, pp. 249-259
-
-
Nagasaki, T.1
Hojo, M.2
Uno, A.3
Satch, T.4
Koumoto, K.5
Mizu, M.6
Sakurai, K.7
Shinkai, S.8
-
109
-
-
0347355380
-
Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficiency
-
doi:10.1016/S0939-6411(03)00155-3
-
Mansouri, S., Lavigne, P., Corsi, K., Benderdour, M., Beaumont, E., Fernandes, J. C. (2004). Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficiency. European Journal of Pharmaceutics and Biopharmaceutics, 57(1), 1-8. doi: 10. 1016/S0939-6411(03)00155-3.
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 1-8
-
-
Mansouri, S.1
Lavigne, P.2
Corsi, K.3
Benderdour, M.4
Beaumont, E.5
Fernandes, J.C.6
-
110
-
-
0034279026
-
Chemical modification of chitosan: binding proprieties of a-galactosyl-chitosan conjugates. Potential inhibitors in acute rejection following xeno-transplantation
-
doi:10.1021/bm005536r
-
Sashiwa, H., Thompson, J. M., Das, S. K., Shigenasa, Y., Tripathy, S., Roy, R. (2000). Chemical modification of chitosan: binding proprieties of a-galactosyl-chitosan conjugates. Potential inhibitors in acute rejection following xeno-transplantation. Biomolecules, 1(3), 303-305. doi: 10. 1021/bm005536r.
-
(2000)
Biomolecules
, vol.1
, Issue.3
, pp. 303-305
-
-
Sashiwa, H.1
Thompson, J.M.2
Das, S.K.3
Shigenasa, Y.4
Tripathy, S.5
Roy, R.6
-
111
-
-
0037568349
-
Separation of enzymes by sequential macroaffinity ligand-facilitated three-phase partitioning
-
doi:10.1016/S0021-9673(03)00522-3
-
Sharma, A., Mondal, K., Gupta, M. N. (2003). Separation of enzymes by sequential macroaffinity ligand-facilitated three-phase partitioning. Journal of Chromatography A, 995(1& 2), 127-134. doi: 10. 1016/S0021-9673(03)00522-3.
-
(2003)
Journal of Chromatography A
, vol.995
, Issue.1-2
, pp. 127-134
-
-
Sharma, A.1
Mondal, K.2
Gupta, M.N.3
-
112
-
-
0345688758
-
Biospecific fractionation of chitosan
-
doi:10.1021/bm034124q
-
Sasaki, C., Kristiansen, A., Fukamizo, T., Varum, K. M. (2003). Biospecific fractionation of chitosan. Biomolecules, 4(6), 1686-1690. doi: 10. 1021/bm034124q.
-
(2003)
Biomolecules
, vol.4
, Issue.6
, pp. 1686-1690
-
-
Sasaki, C.1
Kristiansen, A.2
Fukamizo, T.3
Varum, K.M.4
-
113
-
-
1842535339
-
Incorporation of a high concentration of mineral or vitamin into chitosan-based films
-
doi:10.1021/jf034612p
-
Park, S. I., & Zhao, Y. (2004). Incorporation of a high concentration of mineral or vitamin into chitosan-based films. Journal of Agricultural and Food Chemistry, 52(7), 1933-1939. doi: 10. 1021/jf034612p.
-
(2004)
Journal of Agricultural and Food Chemistry
, vol.52
, Issue.7
, pp. 1933-1939
-
-
Park, S.I.1
Zhao, Y.2
-
114
-
-
48549091594
-
Films based on chitosan polyelectrolyte complexes for skin drug delivery: development and characterisation
-
doi:10.1016/j.memsci.2008.04.011
-
Silva, C. L., Pereira, J. C., Ramalho, A., Pais, A. A. C. C., Sousa, J. S. J. (2008). Films based on chitosan polyelectrolyte complexes for skin drug delivery: development and characterisation. Journal of Membrane Science, 320, 268-279. doi: 10. 1016/j. memsci. 2008. 04. 011.
-
(2008)
Journal of Membrane Science
, vol.320
, pp. 268-279
-
-
Silva, C.L.1
Pereira, J.C.2
Ramalho, A.3
Pais, A.A.C.C.4
Sousa, J.S.J.5
-
115
-
-
0034255170
-
Characterization of thermosensitive chitosan gels for the sustained delivery of drugs
-
doi:10.1016/S0378-5173(00)00428-2
-
Ruel-Gariepy, E., Chenite, A., Chaput, C., Guirguis, S., Lerous, J. (2000). Characterization of thermosensitive chitosan gels for the sustained delivery of drugs. International Journal of Pharmaceutics, 203(1-2), 89-98. doi: 10. 1016/S0378-5173(00)00428-2.
-
(2000)
International Journal of Pharmaceutics
, vol.203
, Issue.1-2
, pp. 89-98
-
-
Ruel-Gariepy, E.1
Chenite, A.2
Chaput, C.3
Guirguis, S.4
Lerous, J.5
-
116
-
-
0035966493
-
The use of chitosan gels as matrices for electrically-modulated drug delivery
-
doi:10.1016/S0168-3659(00)00333-3
-
Ramanathan, S., & Block, L. H. (2001). The use of chitosan gels as matrices for electrically-modulated drug delivery. Journal of Controlled Release, 70(1-2), 109-123. doi: 10. 1016/S0168-3659(00)00333-3.
-
(2001)
Journal of Controlled Release
, vol.70
, Issue.1-2
, pp. 109-123
-
-
Ramanathan, S.1
Block, L.H.2
-
117
-
-
0037122745
-
Synthesis of nanogel carrier for delivery of active phosphorylated nucleoside analogues
-
Vinogradov, S. V., Bronich, T. K., Kabanow, A. V. (2002). Synthesis of nanogel carrier for delivery of active phosphorylated nucleoside analogues. Advanced Drug Delivery Reviews, 54(1), 135-147.
-
(2002)
Advanced Drug Delivery Reviews
, vol.54
, Issue.1
, pp. 135-147
-
-
Vinogradov, S.V.1
Bronich, T.K.2
Kabanow, A.V.3
-
118
-
-
1442348854
-
Therapeutic efficacy of sustained drug release from chitosan gel on local inflammation
-
doi:10.1016/j.ijpharm.2003.11.036
-
Kofuji, K., Akamine, H., Qian, C. J., Watanaba, K., Togan, Y., Nishimura, M., Sugiyana, I., Murata, Y., Kawashima, S. (2004). Therapeutic efficacy of sustained drug release from chitosan gel on local inflammation. International Journal of Pharmaceutics, 272(1-2), 65-78. doi: 10. 1016/j. ijpharm. 2003. 11. 036.
-
(2004)
International Journal of Pharmaceutics
, vol.272
, Issue.1-2
, pp. 65-78
-
-
Kofuji, K.1
Akamine, H.2
Qian, C.J.3
Watanaba, K.4
Togan, Y.5
Nishimura, M.6
Sugiyana, I.7
Murata, Y.8
Kawashima, S.9
-
119
-
-
0346724871
-
Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications
-
doi:10.1016/S0939-6411(03)00160-7
-
Bergera, J., Reista, M., Mayera, J. M., Feltb, O., Gurny, R. (2004). Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications. European Journal of Pharmaceutics and Biopharmaceutics, 57(1), 35-52. doi: 10. 1016/S0939-6411(03)00160-7.
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 35-52
-
-
Bergera, J.1
Reista, M.2
Mayera, J.M.3
Feltb, O.4
Gurny, R.5
-
120
-
-
0037027833
-
Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A
-
doi:10.1016/S0378-5173(02)00461-1
-
El-Shabouri, M. H. (2002). Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A. International Journal of Pharmaceutics, 249, 101-108. doi: 10. 1016/S0378-5173(02)00461-1.
-
(2002)
International Journal of Pharmaceutics
, vol.249
, pp. 101-108
-
-
El-Shabouri, M.H.1
-
121
-
-
0028365910
-
In vitro drug release behavior of d, l-lactide/glycolide copolymer (PLGA) nanospheres with nafarelin acetate prepared by a novel spontaneous emulsification solvent diffusion method
-
doi:10.1002/jps.2600830527
-
Niwa, T., Takeuchi, H., Hino, T., Kunou, N., Kawashima, Y. (1994). In vitro drug release behavior of d, l-lactide/glycolide copolymer (PLGA) nanospheres with nafarelin acetate prepared by a novel spontaneous emulsification solvent diffusion method. Journal of Pharmaceutical Sciences, 83(5), 727-732. doi: 10. 1002/jps. 2600830527.
-
(1994)
Journal of Pharmaceutical Sciences
, vol.83
, Issue.5
, pp. 727-732
-
-
Niwa, T.1
Takeuchi, H.2
Hino, T.3
Kunou, N.4
Kawashima, Y.5
-
122
-
-
0034658305
-
Preparation and evaluation of the in vitro drug release properties and mucoadhesion of novel microspheres of hyaluronic acid and chitosan
-
doi:10.1016/S0168-3659(99)00285-0
-
Lim, S. T., Martin, G. P., Berry, D. J., Brown, M. B. (2000). Preparation and evaluation of the in vitro drug release properties and mucoadhesion of novel microspheres of hyaluronic acid and chitosan. Journal of Controlled Release, 66(2-3), 281-292. doi: 10. 1016/S0168-3659(99)00285-0.
-
(2000)
Journal of Controlled Release
, vol.66
, Issue.2-3
, pp. 281-292
-
-
Lim, S.T.1
Martin, G.P.2
Berry, D.J.3
Brown, M.B.4
-
123
-
-
16244384193
-
Development of a single dose tetanus toxoid formulation based on polymeric microspheres: a comparative study of poly(d, l-lactic-co-glycolic acid) versus chitosan microspheres
-
doi:10.1016/j.ijpharm.2004.12.026
-
Jaganathan, K. S., Rao, Y. U., Singh, P., Prabakaran, D., Gupta, S., Jain, A., Vyas, S. P. (2005). Development of a single dose tetanus toxoid formulation based on polymeric microspheres: a comparative study of poly(d, l-lactic-co-glycolic acid) versus chitosan microspheres. International Journal of Pharmaceutics, 294(1-2), 23-32. doi: 10. 1016/j. ijpharm. 2004. 12. 026.
-
(2005)
International Journal of Pharmaceutics
, vol.294
, Issue.1-2
, pp. 23-32
-
-
Jaganathan, K.S.1
Rao, Y.U.2
Singh, P.3
Prabakaran, D.4
Gupta, S.5
Jain, A.6
Vyas, S.P.7
-
124
-
-
4243321010
-
Alginate in drug delivery systems
-
doi:10.1081/DDC-120003853
-
Tønnesen, H. H., & Karlsen, J. (2002). Alginate in drug delivery systems. Drug Development and Industrial Pharmacy, 28(6), 621-630. doi: 10. 1081/DDC-120003853.
-
(2002)
Drug Development and Industrial Pharmacy
, vol.28
, Issue.6
, pp. 621-630
-
-
Tønnesen, H.H.1
Karlsen, J.2
-
125
-
-
0027438068
-
Development of a new drug carrier made from alginate
-
doi:10.1002/jps.2600820909
-
Rajaonarivony, M., Vauthier, C., Couarraze, G., Puisieux, F., Couvreur, P. (1993). Development of a new drug carrier made from alginate. Journal of Pharmaceutical Sciences, 82(8), 912-917. doi: 10. 1002/jps. 2600820909.
-
(1993)
Journal of Pharmaceutical Sciences
, vol.82
, Issue.8
, pp. 912-917
-
-
Rajaonarivony, M.1
Vauthier, C.2
Couarraze, G.3
Puisieux, F.4
Couvreur, P.5
-
126
-
-
23944517307
-
Nano-encapsulation of azole antifungals: potential applications to improve oral drug delivery
-
doi:10.1016/j.ijpharm.2005.05.027
-
Pandey, R., Ahmad, Z., Sharma, S., Khuller, G. K. (2005). Nano-encapsulation of azole antifungals: potential applications to improve oral drug delivery. International Journal of Pharmaceutics, 301(1-2), 268-276. doi: 10. 1016/j. ijpharm. 2005. 05. 027.
-
(2005)
International Journal of Pharmaceutics
, vol.301
, Issue.1-2
, pp. 268-276
-
-
Pandey, R.1
Ahmad, Z.2
Sharma, S.3
Khuller, G.K.4
-
127
-
-
73649128895
-
Preparation of drug nanoparticles by emulsion evaporation method
-
doi:10.1088/1742-6596/187/1/012047
-
Hoa, L. T. M., Chi, N. T., Triet, N. M., Nhan, L. N. T., Chien, D. M. (2009). Preparation of drug nanoparticles by emulsion evaporation method. Journal of Physics Conference Series, 187, 1-4. doi: 10. 1088/1742-6596/187/1/012047.
-
(2009)
Journal of Physics Conference Series
, vol.187
, pp. 1-4
-
-
Hoa, L.T.M.1
Chi, N.T.2
Triet, N.M.3
Nhan, L.N.T.4
Chien, D.M.5
-
128
-
-
0006779082
-
A survey of the study objects in this volume
-
H. R. Kruyt (Ed.), Amsterdam: Elsevier
-
Bungenberg de Jong, H. G. (1949). A survey of the study objects in this volume. In H. R. Kruyt (Ed.), Colloid science vol II (pp. 1-18). Amsterdam: Elsevier.
-
(1949)
Colloid Science Vol II
, pp. 1-18
-
-
Bungenberg de Jong, H.G.1
-
129
-
-
0029814816
-
Modulation of protein release from chitosan-alginate microcapsules using pH- sensitive polymer hydroxypropyl methylcellulose acetate succinate
-
doi:10.3109/02652049609026035
-
Okhamafe, A. O., Amsden, B., Chu, W., Goosen, M. F. A. (1996). Modulation of protein release from chitosan-alginate microcapsules using pH- sensitive polymer hydroxypropyl methylcellulose acetate succinate. Journal of Microencapsulation, 13(5), 497-508. doi: 10. 3109/02652049609026035.
-
(1996)
Journal of Microencapsulation
, vol.13
, Issue.5
, pp. 497-508
-
-
Okhamafe, A.O.1
Amsden, B.2
Chu, W.3
Goosen, M.F.A.4
-
130
-
-
0031939288
-
Influence of chitosan microspheres on the transport of prednisone sodium phosphate across HT-29 cell monolayers
-
doi:10.1023/A:1011996619500
-
Mooren, F. C., & Berthold, A. (1998). Influence of chitosan microspheres on the transport of prednisone sodium phosphate across HT-29 cell monolayers. Pharmaceutical Research, 15(1), 58-65. doi: 10. 1023/A: 1011996619500.
-
(1998)
Pharmaceutical Research
, vol.15
, Issue.1
, pp. 58-65
-
-
Mooren, F.C.1
Berthold, A.2
-
131
-
-
33749589427
-
Formation of self-organized nanoparticles by lecithin/chitosan ionic interaction
-
doi:10.1016/j.ijpharm.2006.06.036
-
Sonvico, F., Cagnani, A., Rossi, A., Motta, S., Di Bari, M. T., Cavatorta, F., Alonso, M. J., Deriu, A., et al. (2006). Formation of self-organized nanoparticles by lecithin/chitosan ionic interaction. The International Journal of Pharmaceutics, 324(1), 67-73. doi: 10. 1016/j. ijpharm. 2006. 06. 036.
-
(2006)
The International Journal of Pharmaceutics
, vol.324
, Issue.1
, pp. 67-73
-
-
Sonvico, F.1
Cagnani, A.2
Rossi, A.3
Motta, S.4
Di Bari, M.T.5
Cavatorta, F.6
Alonso, M.J.7
Deriu, A.8
-
132
-
-
0032580495
-
DNA-polycation nanospheres as non-viral gene delivery vehicles
-
doi:10.1016/S0168-3659(97)00252-6
-
Leong, K. W., Mao, H. Q., Truong-Le, V. L., Roy, K., Walsh, S. M., August, J. T. (1998). DNA-polycation nanospheres as non-viral gene delivery vehicles. Journal of Controlled Release, 53(1-3), 183-193. doi: 10. 1016/S0168-3659(97)00252-6.
-
(1998)
Journal of Controlled Release
, vol.53
, Issue.1-3
, pp. 183-193
-
-
Leong, K.W.1
Mao, H.Q.2
Truong-Le, V.L.3
Roy, K.4
Walsh, S.M.5
August, J.T.6
-
133
-
-
0032958073
-
Oral gene delivery with chitosan-DNA nanoparticles generates immunologic protection in a murine model of peanut allergy
-
doi:10.1038/7385
-
Roy, K., Mao, H. Q., Huang, S. K., Leong, K. W. (1999). Oral gene delivery with chitosan-DNA nanoparticles generates immunologic protection in a murine model of peanut allergy. Nature Medicine, 5(4), 387-391. doi: 10. 1038/7385.
-
(1999)
Nature Medicine
, vol.5
, Issue.4
, pp. 387-391
-
-
Roy, K.1
Mao, H.Q.2
Huang, S.K.3
Leong, K.W.4
-
134
-
-
34548625240
-
Chitosan and lactic acid-grafted chitosan nanoparticles as carriers for prolonged drug delivery
-
doi:10.2147/nano.2006.1.2.18
-
Bhattarai, N., Ramay, H. R., Chou, S. H., Zhang, M. (2006). Chitosan and lactic acid-grafted chitosan nanoparticles as carriers for prolonged drug delivery. International Journal of Nanomedicine, 1(2), 181-187. doi: 10. 2147/nano. 2006. 1. 2. 18.
-
(2006)
International Journal of Nanomedicine
, vol.1
, Issue.2
, pp. 181-187
-
-
Bhattarai, N.1
Ramay, H.R.2
Chou, S.H.3
Zhang, M.4
-
135
-
-
0242352525
-
N-acylated chitosan: hydrophobic matrices for controlled drug release
-
doi:10.1016/S0168-3659(03)00327-4
-
Tien, C. L., Lacroix, I.-S. P., Mateescu, M. A. (2003). N-acylated chitosan: hydrophobic matrices for controlled drug release. Journal of Controlled Release, 93(1), 1-13. doi: 10. 1016/S0168-3659(03)00327-4.
-
(2003)
Journal of Controlled Release
, vol.93
, Issue.1
, pp. 1-13
-
-
Tien, C.L.1
Lacroix, I.-S.P.2
Mateescu, M.A.3
-
136
-
-
13844265668
-
Self -assembled nanoparticles containing hydrophobically modified glycol chitosan for gene delivery
-
doi:10.1016/j.jconrel.2004.11.033
-
Yoo, H. S., Lee, J. E., Chung, H., Kwon, I. C., Jeong, S. Y. (2005). Self -assembled nanoparticles containing hydrophobically modified glycol chitosan for gene delivery. Journal of Controlled Release, 103(1), 235-243. doi: 10. 1016/j. jconrel. 2004. 11. 033.
-
(2005)
Journal of Controlled Release
, vol.103
, Issue.1
, pp. 235-243
-
-
Yoo, H.S.1
Lee, J.E.2
Chung, H.3
Kwon, I.C.4
Jeong, S.Y.5
-
137
-
-
1542614045
-
Self-assembled nanoparticles based on glycol chitosan bearing 5 β-cholanic acid for RGD peptide delivery
-
doi:10.1016/j.jconrel.2003.12.020
-
Park, J. H., Kwon, S., Nam, J. O., et al. (2005). Self-assembled nanoparticles based on glycol chitosan bearing 5 β-cholanic acid for RGD peptide delivery. Journal of Controlled Release, 95(3), 579-588. doi: 10. 1016/j. jconrel. 2003. 12. 020.
-
(2005)
Journal of Controlled Release
, vol.95
, Issue.3
, pp. 579-588
-
-
Park, J.H.1
Kwon, S.2
Nam, J.O.3
-
138
-
-
36549084546
-
Self-assembled nanoparticles based on hydrophobically modified chitosan as carriers for doxorubicin
-
doi:10.1016/j.nano.2007.08.002
-
Zhang, J., Chen, X. G., Li, Y. Y., Liu, C. S. (2007). Self-assembled nanoparticles based on hydrophobically modified chitosan as carriers for doxorubicin. Nanomedicine, 3(4), 258-265. doi: 10. 1016/j. nano. 2007. 08. 002.
-
(2007)
Nanomedicine
, vol.3
, Issue.4
, pp. 258-265
-
-
Zhang, J.1
Chen, X.G.2
Li, Y.Y.3
Liu, C.S.4
-
139
-
-
40649100957
-
Antitumor efficacy of cisplatin-loaded glycol chitosan nanoparticles in tumor-bearing mice
-
doi:10.1016/j.jconrel.2007.12.014
-
Kim, J. H., Kim, Y. S., Park, K., et al. (2008). Antitumor efficacy of cisplatin-loaded glycol chitosan nanoparticles in tumor-bearing mice. Journal of Controlled Release, 127(1), 41-49. doi: 10. 1016/j. jconrel. 2007. 12. 014.
-
(2008)
Journal of Controlled Release
, vol.127
, Issue.1
, pp. 41-49
-
-
Kim, J.H.1
Kim, Y.S.2
Park, K.3
-
140
-
-
77649184038
-
Effects of lipophilic emulsifiers on the oral administration of lovastatin from nanostructured lipid carriers: physicochemical characterization and pharmacokinetics
-
doi:10.1016/j.ejpb.2009.12.008
-
Chen, C. C., Tsai, T. H., Huang, Z. R., Fang, J. F. (2010). Effects of lipophilic emulsifiers on the oral administration of lovastatin from nanostructured lipid carriers: physicochemical characterization and pharmacokinetics. European Journal of Pharmaceutics and Biopharmaceutics, 74(3), 474-482. doi: 10. 1016/j. ejpb. 2009. 12. 008.
-
(2010)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.74
, Issue.3
, pp. 474-482
-
-
Chen, C.C.1
Tsai, T.H.2
Huang, Z.R.3
Fang, J.F.4
-
141
-
-
34547969073
-
Nanostructured lipid carriers (NLC) in cosmetic dermal products
-
doi:10.1016/j.addr.2007.04.012
-
Müller, R. H., Petersen, R. D., Hommoss, A., Pardeike, J. (2007). Nanostructured lipid carriers (NLC) in cosmetic dermal products. Advanced Drug Delivery Reviews, 59(6), 522-530. doi: 10. 1016/j. addr. 2007. 04. 012.
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, Issue.6
, pp. 522-530
-
-
Müller, R.H.1
Petersen, R.D.2
Hommoss, A.3
Pardeike, J.4
-
142
-
-
0345863541
-
Mechanistic study of the uptake of wheat germ agglutinin-conjugated PLGA nano particles by A549 cells
-
doi:10.1002/jps.10507
-
Mo, Y., & Lim, L. (2004). Mechanistic study of the uptake of wheat germ agglutinin-conjugated PLGA nano particles by A549 cells. Journal of Pharmaceutical Sciences, 93(1), 20-28. doi: 10. 1002/jps. 10507.
-
(2004)
Journal of Pharmaceutical Sciences
, vol.93
, Issue.1
, pp. 20-28
-
-
Mo, Y.1
Lim, L.2
-
143
-
-
21244483540
-
Formulating paclitaxel in nanoparticles alters its disposition
-
doi:10.1007/s11095-005-4581-4
-
Yeh, T. K., Lu, Z., Wientjes, M. G., Au, J. L.-S. (2005). Formulating paclitaxel in nanoparticles alters its disposition. Pharmaceutical Research, 22(6), 867-874. doi: 10. 1007/s11095-005-4581-4.
-
(2005)
Pharmaceutical Research
, vol.22
, Issue.6
, pp. 867-874
-
-
Yeh, T.K.1
Lu, Z.2
Wientjes, M.G.3
Au, J.L.-S.4
-
144
-
-
1442350542
-
Synthesis and evaluation of a hematoporphyrin derivative in a folate receptor-targeted solid-lipid nanoparticle formulation
-
doi:0250-7005/2004$2.00+.40
-
Stevens, P. J., Sekido, M., Lee, R. J. (2004). Synthesis and evaluation of a hematoporphyrin derivative in a folate receptor-targeted solid-lipid nanoparticle formulation. Anticancer Research, 24(1), 161-165. doi: 0250-7005/2004$2. 00+. 40.
-
(2004)
Anticancer Research
, vol.24
, Issue.1
, pp. 161-165
-
-
Stevens, P.J.1
Sekido, M.2
Lee, R.J.3
-
145
-
-
17644366858
-
A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug
-
doi:10.1007/s11095-004-7667-5
-
Stevens, P. J., Sekido, M., Lee, R. J. (2004). A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug. Pharmaceutical Research, 21(12), 2153-2157. doi: 10. 1007/s11095-004-7667-5.
-
(2004)
Pharmaceutical Research
, vol.21
, Issue.12
, pp. 2153-2157
-
-
Stevens, P.J.1
Sekido, M.2
Lee, R.J.3
-
146
-
-
34250337519
-
Lipid-based nanoparticulate drug delivery systems
-
1st edn., D. Thassu, M. Deleers, and Y. Pathak (Eds.), New York: Informa Healthcare USA, Inc
-
Wu, J., Xiaobin, Z., Lee, R. J. (2007). Lipid-based nanoparticulate drug delivery systems. In D. Thassu, M. Deleers, & Y. Pathak (Eds.), Nanoparticulate drug delivery systems (1st ed.). New York: Informa Healthcare USA, Inc.
-
(2007)
Nanoparticulate Drug Delivery Systems
-
-
Wu, J.1
Xiaobin, Z.2
Lee, R.J.3
-
147
-
-
77951690744
-
Lipid-based nanoparticles as pharmaceutical drug carriers: from concepts to clinic
-
Puri, A., Loomis, K., Smith, B., et al. (2009). Lipid-based nanoparticles as pharmaceutical drug carriers: from concepts to clinic. Critical Reviews in Therapeutic Drug Carrier Systems, 26(6), 523-580.
-
(2009)
Critical Reviews in Therapeutic Drug Carrier Systems
, vol.26
, Issue.6
, pp. 523-580
-
-
Puri, A.1
Loomis, K.2
Smith, B.3
-
148
-
-
0037677618
-
The influence of solid lipid nanoparticles on skin hydration and viscoelasticity-in vivo study
-
doi:10.1016/j.addr.2003.12.002
-
Wissing, S. A., & Muller, R. H. (2003). The influence of solid lipid nanoparticles on skin hydration and viscoelasticity-in vivo study. European Journal of Pharmaceutics and Biopharmaceutics, 56(1), 67-72. doi: 10. 1016/j. addr. 2003. 12. 002.
-
(2003)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.56
, Issue.1
, pp. 67-72
-
-
Wissing, S.A.1
Muller, R.H.2
-
149
-
-
1942453805
-
Solid lipid nanoparticles for parenteral drug delivery
-
doi:10.1016/j.addr.2003.12.002
-
Wissing, S. A., Kayser, O., Muller, R. H. (2004). Solid lipid nanoparticles for parenteral drug delivery. Advanced Drug Delivery Reviews, 56(9), 1257-1272. doi: 10. 1016/j. addr. 2003. 12. 002.
-
(2004)
Advanced Drug Delivery Reviews
, vol.56
, Issue.9
, pp. 1257-1272
-
-
Wissing, S.A.1
Kayser, O.2
Muller, R.H.3
-
150
-
-
0036297426
-
A novel phase inversion-based process for the preparation of lipid nanocarriers
-
doi:10.1023/A:1016121319668
-
Heurtault, B., Saulnier, P., Pech, B., Proust, J. E., Benoit, J. P. (2002). A novel phase inversion-based process for the preparation of lipid nanocarriers. Pharmaceutical Research, 19(6), 875-880. doi: 10. 1023/A: 1016121319668.
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.6
, pp. 875-880
-
-
Heurtault, B.1
Saulnier, P.2
Pech, B.3
Proust, J.E.4
Benoit, J.P.5
-
151
-
-
26944493750
-
Preparation of solid lipid nanoparticles using a membrane contactor
-
doi:10.1016/j.jconrel.2005.07.023
-
Charcosset, C., El-Harati, A., Fessi, H. (2005). Preparation of solid lipid nanoparticles using a membrane contactor. Journal of Controlled Release, 108(1), 112-120. doi: 10. 1016/j. jconrel. 2005. 07. 023.
-
(2005)
Journal of Controlled Release
, vol.108
, Issue.1
, pp. 112-120
-
-
Charcosset, C.1
El-Harati, A.2
Fessi, H.3
-
152
-
-
0028285718
-
Solid lipid nanoparticles (SLN) for controlled drug delivery: I. Production, characterization and sterilization
-
doi:10.1016/0168-3659(94)90047-7
-
Schwarz, C., Mehnert, W., Lucks, J. S., Muller, R. H. (1994). Solid lipid nanoparticles (SLN) for controlled drug delivery: I. Production, characterization and sterilization. Journal of Controlled Release, 30, 83-96. doi: 10. 1016/0168-3659(94)90047-7.
-
(1994)
Journal of Controlled Release
, vol.30
, pp. 83-96
-
-
Schwarz, C.1
Mehnert, W.2
Lucks, J.S.3
Muller, R.H.4
-
153
-
-
0030866983
-
Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential
-
doi:10.1016/S0168-3659(97)00046-1
-
Westesen, K., Bunjes, H., Koch, M. H. J. (1997). Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential. Journal of Controlled Release, 48, 223-236. doi: 10. 1016/S0168-3659(97)00046-1.
-
(1997)
Journal of Controlled Release
, vol.48
, pp. 223-236
-
-
Westesen, K.1
Bunjes, H.2
Koch, M.H.J.3
-
154
-
-
51049120877
-
Importance of solid lipid nanoparticles (SLN) in various administration routes and future perspectives
-
Uner, M., & Yener, G. (2007). Importance of solid lipid nanoparticles (SLN) in various administration routes and future perspectives. International Journal of Nanomedicine, 2(3), 289-300.
-
(2007)
International Journal of Nanomedicine
, vol.2
, Issue.3
, pp. 289-300
-
-
Uner, M.1
Yener, G.2
-
155
-
-
79953234715
-
Preparation and evaluation of solid lipid nanoparticles of baicalin for ocular drug delivery system in vitro and in vivo
-
doi:10.3109/03639045.2010.522193
-
Liu, Z., Zhang, X., Wu, H., Li, J., Shu, L., Liu, R., Li, L., Li, N. (2011). Preparation and evaluation of solid lipid nanoparticles of baicalin for ocular drug delivery system in vitro and in vivo. Drug Development and Industrial Pharmacy, 37(4), 475-481. doi: 10. 3109/03639045. 2010. 522193.
-
(2011)
Drug Development and Industrial Pharmacy
, vol.37
, Issue.4
, pp. 475-481
-
-
Liu, Z.1
Zhang, X.2
Wu, H.3
Li, J.4
Shu, L.5
Liu, R.6
Li, L.7
Li, N.8
-
156
-
-
79955670424
-
In vitro evaluation of idebenone-loaded solid lipid nanoparticles for drug delivery to the brain
-
Montenegro, L., Campisi, A., Sarpietro, M. G., et al. (2011). In vitro evaluation of idebenone-loaded solid lipid nanoparticles for drug delivery to the brain. Drug Dev Ind Pharm, 37(6), 737-746.
-
(2011)
Drug Dev Ind Pharm
, vol.37
, Issue.6
, pp. 737-746
-
-
Montenegro, L.1
Campisi, A.2
Sarpietro, M.G.3
-
157
-
-
77956161610
-
Solid lipid nanoparticles for ocular drug delivery
-
doi:10.3109/10717544.2010.483257
-
Seyfoddin, A., Shaw, J., Al-Kassas, R. (2010). Solid lipid nanoparticles for ocular drug delivery. Drug Delivery, 17(7), 467-489. doi: 10. 3109/10717544. 2010. 483257.
-
(2010)
Drug Delivery
, vol.17
, Issue.7
, pp. 467-489
-
-
Seyfoddin, A.1
Shaw, J.2
Al-Kassas, R.3
-
158
-
-
77549083354
-
Solid lipid nanoparticles as anti-inflammatory drug delivery system in a human inflammatory bowel disease whole-blood model
-
doi:10.1016/j.ejps.2010.01.013
-
Serpe, L., Canaparo, R., Daperno, M., Sostegni, R., Martinasso, G., Muntoni, E., Ippolito, L., Vivenza, N., Pera, A., Eandi, M., Gasco, M. R., Zara, G. P. (2010). Solid lipid nanoparticles as anti-inflammatory drug delivery system in a human inflammatory bowel disease whole-blood model. European Journal of Pharmaceutical Sciences, 39(5), 428-436. doi: 10. 1016/j. ejps. 2010. 01. 013.
-
(2010)
European Journal of Pharmaceutical Sciences
, vol.39
, Issue.5
, pp. 428-436
-
-
Serpe, L.1
Canaparo, R.2
Daperno, M.3
Sostegni, R.4
Martinasso, G.5
Muntoni, E.6
Ippolito, L.7
Vivenza, N.8
Pera, A.9
Eandi, M.10
Gasco, M.R.11
Zara, G.P.12
-
159
-
-
47949106574
-
Reversal activity of nanostructured lipid carriers loading cytotoxic drug in multi-drug resistant cancer cells
-
doi:10.1016/j.ijpharm.2008.06.002
-
Zhang, X. G., Miao, J., Dai, Y. Q., Du, Y. Z., Yuan, H., Hu, F. Q. (2008). Reversal activity of nanostructured lipid carriers loading cytotoxic drug in multi-drug resistant cancer cells. International Journal of Pharmaceutics, 361(1-2), 239-244. doi: 10. 1016/j. ijpharm. 2008. 06. 002.
-
(2008)
International Journal of Pharmaceutics
, vol.361
, Issue.1-2
, pp. 239-244
-
-
Zhang, X.G.1
Miao, J.2
Dai, Y.Q.3
Du, Y.Z.4
Yuan, H.5
Hu, F.Q.6
-
160
-
-
34447305482
-
Encapsulation of ascorbylpalmitate in nanostructured lipid carriers (NLC)-effects of formulation parameters on physicochemical stability
-
doi:10.1016/j.ijpharm.2007.03.022
-
Teeranachaideekul, V., Muller, R. H., Junyaprasert, V. B. (2007). Encapsulation of ascorbylpalmitate in nanostructured lipid carriers (NLC)-effects of formulation parameters on physicochemical stability. International Journal of Pharmaceutics, 340(1-2), 198-206. doi: 10. 1016/j. ijpharm. 2007. 03. 022.
-
(2007)
International Journal of Pharmaceutics
, vol.340
, Issue.1-2
, pp. 198-206
-
-
Teeranachaideekul, V.1
Muller, R.H.2
Junyaprasert, V.B.3
-
161
-
-
35648975238
-
Preparation and characteristics of nanostructured lipid carriers for control-releasing progesterone by melt-emulsification
-
doi:10.1016/j.colsurfb.2007.06.011
-
Yuan, H., Wang, L. L., Du, Y. Z., You, J., Hu, F. Q., Zeng, S. (2007). Preparation and characteristics of nanostructured lipid carriers for control-releasing progesterone by melt-emulsification. Colloids and Surfaces. B, Biointerfaces, 60(2), 174-179. doi: 10. 1016/j. colsurfb. 2007. 06. 011.
-
(2007)
Colloids and Surfaces. B, Biointerfaces
, vol.60
, Issue.2
, pp. 174-179
-
-
Yuan, H.1
Wang, L.L.2
Du, Y.Z.3
You, J.4
Hu, F.Q.5
Zeng, S.6
-
162
-
-
0343618485
-
Characterization of a novel solid lipid nanoparticle carrier system based on binary mixtures of liquid and solid lipids
-
doi:10.1016/S0378-5173(00)00378-1
-
Jenning, V., Thunemann, A. F., Gohla, S. H. (2000). Characterization of a novel solid lipid nanoparticle carrier system based on binary mixtures of liquid and solid lipids. International Journal of Pharmaceutics, 1999, 167-177. doi: 10. 1016/S0378-5173(00)00378-1.
-
(2000)
International Journal of Pharmaceutics
, vol.1999
, pp. 167-177
-
-
Jenning, V.1
Thunemann, A.F.2
Gohla, S.H.3
-
164
-
-
33748498943
-
Formulation and evaluation of nanostructured lipid carrier (NLC)-based gel of Valdecoxib
-
Joshi, M., & Patravale, M. (2006). Formulation and evaluation of nanostructured lipid carrier (NLC)-based gel of Valdecoxib. Drug Development and Industrial Pharmacy, 32(8), 911-918.
-
(2006)
Drug Development and Industrial Pharmacy
, vol.32
, Issue.8
, pp. 911-918
-
-
Joshi, M.1
Patravale, M.2
-
165
-
-
0035910874
-
The role of plasma proteins in brain targeting: species dependent protein adsorption patterns on brain-specific lipid drug conjugate (LDC) nanoparticles
-
doi:10.1016/S0378-5173(00)00639-6
-
Geßner, A., Olbrich, C., Schroder, W., Kayser, O., Muller, R. H. (2001). The role of plasma proteins in brain targeting: species dependent protein adsorption patterns on brain-specific lipid drug conjugate (LDC) nanoparticles. International Journal of Pharmaceutics, 214(1-2), 87-91. doi: 10. 1016/S0378-5173(00)00639-6.
-
(2001)
International Journal of Pharmaceutics
, vol.214
, Issue.1-2
, pp. 87-91
-
-
Geßner, A.1
Olbrich, C.2
Schroder, W.3
Kayser, O.4
Muller, R.H.5
-
166
-
-
36649036321
-
Steric stabilization of lipid/polymer particle assemblies by poly(ethylene glycol)-lipids
-
doi:10.1021/bm700753q
-
Thevenot, J., TroutierAL, D. L., Delair, T., Ladaviere, C. (2007). Steric stabilization of lipid/polymer particle assemblies by poly(ethylene glycol)-lipids. Biomacromolecules, 8, 3651-3660. doi: 10. 1021/bm700753q.
-
(2007)
Biomacromolecules
, vol.8
, pp. 3651-3660
-
-
Thevenot, J.1
Troutieral, D.L.2
Delair, T.3
Ladaviere, C.4
-
167
-
-
51849084844
-
Self-assembled lipid-polymer hybrid nanoparticles: a robust drug delivery platform
-
doi:10.1021/nn800275r
-
Zhang, L., Chan, J. M., Gu, F. X., Rhee, J. W., Wang, A. Z., Radovic-Moreno, A. F., et al. (2008). Self-assembled lipid-polymer hybrid nanoparticles: a robust drug delivery platform. ACS Nano, 2, 1696-1702. doi: 10. 1021/nn800275r.
-
(2008)
ACS Nano
, vol.2
, pp. 1696-1702
-
-
Zhang, L.1
Chan, J.M.2
Gu, F.X.3
Rhee, J.W.4
Wang, A.Z.5
Radovic-Moreno, A.F.6
-
168
-
-
76649118810
-
Spatio-temporal controlled delivery of nanoparticles to injured vasculature
-
doi:10.1073/pnas.0914585107
-
Chan, J. M., Zhang, L. F., Tong, R., Ghosh, D., Gao, W., et al. (2010). Spatio-temporal controlled delivery of nanoparticles to injured vasculature. Proceedings of the National Academy of Sciences, 107(5), 2213-2218. doi: 10. 1073/pnas. 0914585107.
-
(2010)
Proceedings of the National Academy of Sciences
, vol.107
, Issue.5
, pp. 2213-2218
-
-
Chan, J.M.1
Zhang, L.F.2
Tong, R.3
Ghosh, D.4
Gao, W.5
-
169
-
-
78649907651
-
Modified nanoprecipitation method for preparation of cytarabine-loaded PLGA nanoparticles
-
doi:10.1208/s12249-010-9519-4
-
Yadav, K. S., & Sawant, K. K. (2010). Modified nanoprecipitation method for preparation of cytarabine-loaded PLGA nanoparticles. AAPS PharmSciTech, 11(3), 1456-1465. doi: 10. 1208/s12249-010-9519-4.
-
(2010)
AAPS PharmSciTech
, vol.11
, Issue.3
, pp. 1456-1465
-
-
Yadav, K.S.1
Sawant, K.K.2
-
170
-
-
78650410138
-
Quick synthesis of lipid-polymer hybrid nanoparticles with low polydispersity using a single-step sonication method
-
doi:10.1021/la103576a
-
Fang, R. H., Aryal, S., Hu, C. M., Zhang, L. (2010). Quick synthesis of lipid-polymer hybrid nanoparticles with low polydispersity using a single-step sonication method. Langmuir, 26(22), 16958-16962. doi: 10. 1021/la103576a.
-
(2010)
Langmuir
, vol.26
, Issue.22
, pp. 16958-16962
-
-
Fang, R.H.1
Aryal, S.2
Hu, C.M.3
Zhang, L.4
-
171
-
-
78649318271
-
Development of novel self-assembled DS-PLGA hybrid nanoparticles for improving oral bioavailability of vincristine sulfate by P-gp inhibition
-
doi:10.1016/j.jconrel.2010.08.010
-
Ling, G., Zhang, P., Zhang, W., Sun, J., et al. (2010). Development of novel self-assembled DS-PLGA hybrid nanoparticles for improving oral bioavailability of vincristine sulfate by P-gp inhibition. Journal of Controlled Release, 148(2), 241-248. doi: 10. 1016/j. jconrel. 2010. 08. 010.
-
(2010)
Journal of Controlled Release
, vol.148
, Issue.2
, pp. 241-248
-
-
Ling, G.1
Zhang, P.2
Zhang, W.3
Sun, J.4
-
172
-
-
47949120334
-
Biofunctionalized targeted nanoparticles for therapeutic applications
-
doi:10.1517/14712598.8.8.1063
-
Wang, A. Z., Gu, F., Zhang, L., Chan, J. M., Radovic-Moreno, A., Shaikh, M. R., Farokhzad, O. C. (2008). Biofunctionalized targeted nanoparticles for therapeutic applications. Expert Opinion on Biological Therapy, 8(8), 1063-1070. doi: 10. 1517/14712598. 8. 8. 1063.
-
(2008)
Expert Opinion on Biological Therapy
, vol.8
, Issue.8
, pp. 1063-1070
-
-
Wang, A.Z.1
Gu, F.2
Zhang, L.3
Chan, J.M.4
Radovic-Moreno, A.5
Shaikh, M.R.6
Farokhzad, O.C.7
-
173
-
-
77953264383
-
Half-antibody functionalized lipid-polymer hybrid nanoparticles for targeted drug delivery to carcino embryonic antigen (CEA) presenting pancreatic cancer cells
-
doi:10.1021/mp900316a
-
Hu, C. M. J., Kaushal, S., Cao, H. S. T., Aryal, S., Sartor, M., et al. (2010). Half-antibody functionalized lipid-polymer hybrid nanoparticles for targeted drug delivery to carcino embryonic antigen (CEA) presenting pancreatic cancer cells. Molecular Pharmaceutics, 7(3), 914-920. doi: 10. 1021/mp900316a.
-
(2010)
Molecular Pharmaceutics
, vol.7
, Issue.3
, pp. 914-920
-
-
Hu, C.M.J.1
Kaushal, S.2
Cao, H.S.T.3
Aryal, S.4
Sartor, M.5
-
174
-
-
77952198864
-
A novel polymer-lipid hybrid nanoparticle for efficient non-viral gene delivery
-
doi:10.1038/aps.2010.15
-
Li, J., Ying-zi He, Y., Li, W., Shen, Y., Li, Y., Wang, Y. (2010). A novel polymer-lipid hybrid nanoparticle for efficient non-viral gene delivery. Acta Pharmacologica Sinica, 31, 509-514. doi: 10. 1038/aps. 2010. 15.
-
(2010)
Acta Pharmacologica Sinica
, vol.31
, pp. 509-514
-
-
Li, J.1
Ying-zi He, Y.2
Li, W.3
Shen, Y.4
Li, Y.5
Wang, Y.6
-
175
-
-
23144456813
-
Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system
-
doi:10.1038/nature03794
-
Sengupta, S., Eavarone, D., Capila, I., Zhao, G., Watson, N., Kiziltepe, T., Sasisekharan, R. (2005). Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system. Nature, 436(7050), 568-572. doi: 10. 1038/nature03794.
-
(2005)
Nature
, vol.436
, Issue.7050
, pp. 568-572
-
-
Sengupta, S.1
Eavarone, D.2
Capila, I.3
Zhao, G.4
Watson, N.5
Kiziltepe, T.6
Sasisekharan, R.7
-
176
-
-
70449530844
-
Folic acid conjugated nanoparticles of mixed lipid monolayer shell and biodegradable polymer core for targeted delivery of Docetaxel
-
doi:10.1016/j.biomaterials.2009.09.036
-
Yiu, T., Li, K., Li, P. J., Liu, B., Feng, S. S. (2010). Folic acid conjugated nanoparticles of mixed lipid monolayer shell and biodegradable polymer core for targeted delivery of Docetaxel. Biomaterials, 31, 330-338. doi: 10. 1016/j. biomaterials. 2009. 09. 036.
-
(2010)
Biomaterials
, vol.31
, pp. 330-338
-
-
Yiu, T.1
Li, K.2
Li, P.J.3
Liu, B.4
Feng, S.S.5
-
177
-
-
60549109846
-
Immunocompatibility properties of lipid-polymer hybrid nanoparticles with heterogeneous surface functional groups
-
doi:10.1016/j.biomaterials.2009.01.005
-
Salvador-Morales, C., Zhang, L., Langer, R., Farokhzad, O. C. (2009). Immunocompatibility properties of lipid-polymer hybrid nanoparticles with heterogeneous surface functional groups. Biomaterials, 30, 2231-2240. doi: 10. 1016/j. biomaterials. 2009. 01. 005.
-
(2009)
Biomaterials
, vol.30
, pp. 2231-2240
-
-
Salvador-Morales, C.1
Zhang, L.2
Langer, R.3
Farokhzad, O.C.4
-
178
-
-
0037462997
-
Biodegradable nanoparticles for drug and gene delivery to cells and tissue
-
doi:10.1016/S0169-409X(02)00228-4
-
Panyam, J., & Labhasetwar, V. (2003). Biodegradable nanoparticles for drug and gene delivery to cells and tissue. Advanced Drug Delivery Reviews, 55(3), 329-347. doi: 10. 1016/S0169-409X(02)00228-4.
-
(2003)
Advanced Drug Delivery Reviews
, vol.55
, Issue.3
, pp. 329-347
-
-
Panyam, J.1
Labhasetwar, V.2
-
179
-
-
0031469673
-
The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent
-
doi:10.1023/A:1012126301290
-
Desai, M. P., Labhasetwar, V., Walter, E., Levy, R. J., Amidon, G. L. (1997). The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent. Pharmaceutical Research, 14(11), 1568-1573. doi: 10. 1023/A: 1012126301290.
-
(1997)
Pharmaceutical Research
, vol.14
, Issue.11
, pp. 1568-1573
-
-
Desai, M.P.1
Labhasetwar, V.2
Walter, E.3
Levy, R.J.4
Amidon, G.L.5
-
180
-
-
0030471901
-
Gastrointestinal uptake of biodegradable microparticles: effect of particle size
-
doi:10.1023/A:1016085108889
-
Desai, M. P., Labhasetwar, V., Amidon, G. L., Levy, R. J. (1996). Gastrointestinal uptake of biodegradable microparticles: effect of particle size. Pharmaceutical Research, 13(12), 1838-1845. doi: 10. 1023/A: 1016085108889.
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.12
, pp. 1838-1845
-
-
Desai, M.P.1
Labhasetwar, V.2
Amidon, G.L.3
Levy, R.J.4
-
181
-
-
0035848402
-
In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density
-
doi:10.1016/S0168-3659(00)00358-8
-
Zauner, W., Farrow, N. A., Haines, A. M. (2001). In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density. Journal of Controlled Release, 71(1), 39-51. doi: 10. 1016/S0168-3659(00)00358-8.
-
(2001)
Journal of Controlled Release
, vol.71
, Issue.1
, pp. 39-51
-
-
Zauner, W.1
Farrow, N.A.2
Haines, A.M.3
-
182
-
-
0035936975
-
Drug delivery in poly(lactide-co-glycolide) nanoparticles surface modified with poloxamer 407 and poloxamine 908: in vitro characterisation and in vivo evaluation
-
doi:10.1023/A:1022604120952
-
Redhead, H. M., Davis, S. S., Illum, L. (2001). Drug delivery in poly(lactide-co-glycolide) nanoparticles surface modified with poloxamer 407 and poloxamine 908: in vitro characterisation and in vivo evaluation. Journal of Controlled Release, 70(3), 353-363. doi: 10. 1023/A: 1022604120952.
-
(2001)
Journal of Controlled Release
, vol.70
, Issue.3
, pp. 353-363
-
-
Redhead, H.M.1
Davis, S.S.2
Illum, L.3
-
183
-
-
46349098694
-
Strategies for enhanced drug delivery to the central nervous system
-
doi:10.4103/0250-474X.41446
-
Dwibhashyam, V. S. N. M., & Nagappa, A. N. (2008). Strategies for enhanced drug delivery to the central nervous system. Indian Journal of Pharmaceutical Sciences, 70(2), 145-153. doi: 10. 4103/0250-474X. 41446.
-
(2008)
Indian Journal of Pharmaceutical Sciences
, vol.70
, Issue.2
, pp. 145-153
-
-
Dwibhashyam, V.S.N.M.1
Nagappa, A.N.2
-
184
-
-
0037335187
-
Direct evidence that polysorbate-80-coated poly(butylcyanoacrylate) nanoparticles deliver drugs to the CNS via specific mechanisms requiring prior binding of drug to the nanoparticles
-
doi:10.1023/A:1022604120952
-
Kreuter, J., Ramge, P., Petrov, V., Hamm, S., Gelperina, S. E., Engelhardt, B., Alyautdin, R., von Briesen, H., Begley, D. J. (2003). Direct evidence that polysorbate-80-coated poly(butylcyanoacrylate) nanoparticles deliver drugs to the CNS via specific mechanisms requiring prior binding of drug to the nanoparticles. Pharmaceutical Research, 20(3), 409-416. doi: 10. 1023/A: 1022604120952.
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.3
, pp. 409-416
-
-
Kreuter, J.1
Ramge, P.2
Petrov, V.3
Hamm, S.4
Gelperina, S.E.5
Engelhardt, B.6
Alyautdin, R.7
von Briesen, H.8
Begley, D.J.9
-
185
-
-
0042125467
-
Physicochemical investigations on solid-lipid nanoparticles and on oil loaded solid-lipid nanoparticles: a nuclear magnetic resonance and electron spin resonance study
-
doi:10.1023/A:1025065418309
-
Jores, K., Mehnert, W., Mader, K. (2003). Physicochemical investigations on solid-lipid nanoparticles and on oil loaded solid-lipid nanoparticles: a nuclear magnetic resonance and electron spin resonance study. Pharmaceutical Research, 20, 1274-1283. doi: 10. 1023/A: 1025065418309.
-
(2003)
Pharmaceutical Research
, vol.20
, pp. 1274-1283
-
-
Jores, K.1
Mehnert, W.2
Mader, K.3
-
186
-
-
12144253184
-
Formulation and characterization of triclosan sub-micronemulsions and nanocapsules
-
doi:10.1080/02652040400015411
-
Maestrell, F., Mura, P., Alonso, M. J. (2004). Formulation and characterization of triclosan sub-micronemulsions and nanocapsules. Journal of Microencapsulation, 21(8), 857-864. doi: 10. 1080/02652040400015411.
-
(2004)
Journal of Microencapsulation
, vol.21
, Issue.8
, pp. 857-864
-
-
Maestrell, F.1
Mura, P.2
Alonso, M.J.3
-
187
-
-
9644312752
-
Physicochemical characterization of protamine-phosphorothioate nanoparticles
-
doi:10.1080/02652040400000504
-
Lochmann, D., Vogel, V., Weyermann, J., et al. (2004). Physicochemical characterization of protamine-phosphorothioate nanoparticles. Journal of Microencapsulation, 21(6), 625-641. doi: 10. 1080/02652040400000504.
-
(2004)
Journal of Microencapsulation
, vol.21
, Issue.6
, pp. 625-641
-
-
Lochmann, D.1
Vogel, V.2
Weyermann, J.3
-
188
-
-
11244273197
-
Long term shelf stability of amphiphilic B-cyclodextrin nanospheres suspensions monitored by dynamic light scattering and cryo-transmission electron microscopy
-
doi:10.1080/02652040400008457%20
-
Geze, A., Putaux, J. L., Choisnard, L., Jehan, P., Wouessidjewe, D. (2004). Long term shelf stability of amphiphilic B-cyclodextrin nanospheres suspensions monitored by dynamic light scattering and cryo-transmission electron microscopy. Journal of Microencapsulation, 21, 607-613. doi: 10. 1080/02652040400008457%20.
-
(2004)
Journal of Microencapsulation
, vol.21
, pp. 607-613
-
-
Geze, A.1
Putaux, J.L.2
Choisnard, L.3
Jehan, P.4
Wouessidjewe, D.5
-
189
-
-
3042551382
-
Bioavailability and pharmacokinetics of cyclosporine A loaded pH-sensitive nanoparticles for oral administration
-
doi:10.1016/j.jconrel.2004.03.003
-
Wang, X., Dai, J., Chen, Z., et al. (2004). Bioavailability and pharmacokinetics of cyclosporine A loaded pH-sensitive nanoparticles for oral administration. Journal of Controlled Release, 97, 421-429. doi: 10. 1016/j. jconrel. 2004. 03. 003.
-
(2004)
Journal of Controlled Release
, vol.97
, pp. 421-429
-
-
Wang, X.1
Dai, J.2
Chen, Z.3
-
190
-
-
54349125120
-
Production and in vitro characterization of solid dosage form incorporating drug nanoparticles
-
doi:10.1080/03639040802005024
-
Muniyappan, S. V. T., Karatgi, P., Prabu, R., Pillai, R. (2008). Production and in vitro characterization of solid dosage form incorporating drug nanoparticles. Drug Development and Industrial Pharmacy, 34(11), 1209-1218. doi: 10. 1080/03639040802005024.
-
(2008)
Drug Development and Industrial Pharmacy
, vol.34
, Issue.11
, pp. 1209-1218
-
-
Muniyappan, S.V.T.1
Karatgi, P.2
Prabu, R.3
Pillai, R.4
-
191
-
-
0842310894
-
Biodegradable nanoparticles containing protein-fatty acid complexes for oral delivery of salmon calcitonin
-
doi:10.1002/jps.10573
-
Yoo, H. S., & Park, T. G. (2004). Biodegradable nanoparticles containing protein-fatty acid complexes for oral delivery of salmon calcitonin. Journal of Pharmaceutical Sciences, 93, 488-495. doi: 10. 1002/jps. 10573.
-
(2004)
Journal of Pharmaceutical Sciences
, vol.93
, pp. 488-495
-
-
Yoo, H.S.1
Park, T.G.2
-
192
-
-
0037523228
-
Visualization of insulin loaded nanocapsules: in vitro and in vivo studies after oral administration to rats
-
doi:10.1023/A:1024470508758
-
Alphandary, H. P., Aboubaker, M., Jaillard, D., Couvreur, P., Vauthier, C. (2003). Visualization of insulin loaded nanocapsules: in vitro and in vivo studies after oral administration to rats. Pharmaceutical Research, 20(7), 1071-1084. doi: 10. 1023/A: 1024470508758.
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.7
, pp. 1071-1084
-
-
Alphandary, H.P.1
Aboubaker, M.2
Jaillard, D.3
Couvreur, P.4
Vauthier, C.5
-
193
-
-
51049092308
-
Factors affecting the clearance and biodistribution of polymeric nanoparticles
-
doi:10.1021/mp800051m
-
Alexis, F., Pridgen, E., Molnar, L. K., Farokhzad, O. C. (2008). Factors affecting the clearance and biodistribution of polymeric nanoparticles. Molecular Pharmaceutics, 5(4), 505-515. doi: 10. 1021/mp800051m.
-
(2008)
Molecular Pharmaceutics
, vol.5
, Issue.4
, pp. 505-515
-
-
Alexis, F.1
Pridgen, E.2
Molnar, L.K.3
Farokhzad, O.C.4
-
194
-
-
49449111729
-
Polymer-supported lipid shells, onions, and flowers
-
doi:10.1039/b804933e
-
Bershteyn, A., Chaparro, J., Yau, R., Kim, M., Reinherz, E., et al. (2008). Polymer-supported lipid shells, onions, and flowers. Soft Matter, 4(9), 1787-1791. doi: 10. 1039/b804933e.
-
(2008)
Soft Matter
, vol.4
, Issue.9
, pp. 1787-1791
-
-
Bershteyn, A.1
Chaparro, J.2
Yau, R.3
Kim, M.4
Reinherz, E.5
-
195
-
-
0032952283
-
PLGA nanoparticles prepared by nanoprecipitation: drug loading and release studies of a water soluble drug
-
doi:10.1016/S0168-3659(98)00116-3
-
Govender, T., Stolnik, S., Garnett, M. C., Illum, L., Davis, S. S. (1999). PLGA nanoparticles prepared by nanoprecipitation: drug loading and release studies of a water soluble drug. Journal of Controlled Release, 57(2), 171-185. doi: 10. 1016/S0168-3659(98)00116-3.
-
(1999)
Journal of Controlled Release
, vol.57
, Issue.2
, pp. 171-185
-
-
Govender, T.1
Stolnik, S.2
Garnett, M.C.3
Illum, L.4
Davis, S.S.5
-
196
-
-
0034630209
-
Defining the drug incorporation properties of PLA-PEG nanoparticles
-
doi:10.1016/S0378-5173(00)00375-6
-
Govender, T., Riley, T., Ehtezazi, T., Garnett, M. C., Stolnik, S., Illum, L., Davis, S. S. (2000). Defining the drug incorporation properties of PLA-PEG nanoparticles. International Journal of Pharmaceutics, 199(1), 95-110. doi: 10. 1016/S0378-5173(00)00375-6.
-
(2000)
International Journal of Pharmaceutics
, vol.199
, Issue.1
, pp. 95-110
-
-
Govender, T.1
Riley, T.2
Ehtezazi, T.3
Garnett, M.C.4
Stolnik, S.5
Illum, L.6
Davis, S.S.7
-
197
-
-
0028050033
-
Synthesis of albumin-dextran sulfate microspheres possessing favourable loading and release characteristics for the anti-cancer doxorubicin
-
doi:10.1016/0168-3659(94)90250-X
-
Chen, Y., McCulloch, R. K., Gray, B. N. (1994). Synthesis of albumin-dextran sulfate microspheres possessing favourable loading and release characteristics for the anti-cancer doxorubicin. Journal of Controlled Release, 31(1), 49-54. doi: 10. 1016/0168-3659(94)90250-X.
-
(1994)
Journal of Controlled Release
, vol.31
, Issue.1
, pp. 49-54
-
-
Chen, Y.1
McCulloch, R.K.2
Gray, B.N.3
-
198
-
-
0030948510
-
PEG-coated nanospheres from amphiphillic diblock and multiblock copolymers: investigation of their drug encapsulation and release characteristics
-
doi:10.1016/S0168-3659(96)01597-0
-
Peracchia, M., Gref, R., Minamitake, Y., Domb, A., Lotan, N., Langer, R. (1997). PEG-coated nanospheres from amphiphillic diblock and multiblock copolymers: investigation of their drug encapsulation and release characteristics. Journal of Controlled Release, 46(3), 223-231. doi: 10. 1016/S0168-3659(96)01597-0.
-
(1997)
Journal of Controlled Release
, vol.46
, Issue.3
, pp. 223-231
-
-
Peracchia, M.1
Gref, R.2
Minamitake, Y.3
Domb, A.4
Lotan, N.5
Langer, R.6
-
199
-
-
75749101439
-
Polymer-cisplatin conjugate nanoparticles for acid-responsive drug delivery
-
doi:10.1021/nn9014032
-
Aryal, S., Hu, C. M. J., Zhang, L. F. (2010). Polymer-cisplatin conjugate nanoparticles for acid-responsive drug delivery. ACS Nano, 4, 251-258. doi: 10. 1021/nn9014032.
-
(2010)
ACS Nano
, vol.4
, pp. 251-258
-
-
Aryal, S.1
Hu, C.M.J.2
Zhang, L.F.3
-
200
-
-
76749124883
-
Silk fibroin nanoparticles for cellular uptake and control release
-
doi:10.1016/j.ijpharm.2009.12.052
-
Kundu, J., Chung, Y. I., Kim, Y. H., Taeb, G., Kundu, S. C. (2010). Silk fibroin nanoparticles for cellular uptake and control release. International Journal of Pharmaceutics, 388(1-2), 242-250. doi: 10. 1016/j. ijpharm. 2009. 12. 052.
-
(2010)
International Journal of Pharmaceutics
, vol.388
, Issue.1-2
, pp. 242-250
-
-
Kundu, J.1
Chung, Y.I.2
Kim, Y.H.3
Taeb, G.4
Kundu, S.C.5
-
201
-
-
0035997341
-
Long-circulating poly(ethylene glycol)-modified gelatin nanoparticles for intracellular delivery
-
doi:10.1023/A:1016486910719
-
Kaul, G., & Amiji, M. (2002). Long-circulating poly(ethylene glycol)-modified gelatin nanoparticles for intracellular delivery. Pharmaceutical Research, 19(7), 1061-1067. doi: 10. 1023/A: 1016486910719.
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.7
, pp. 1061-1067
-
-
Kaul, G.1
Amiji, M.2
-
202
-
-
63649092083
-
Cellular uptake mechanism and intracellular fate of hydrophobically modified glycol chitosan nanoparticles
-
doi:10.1016/j.jconrel.2009.01.018
-
Nam, H. Y., Kwon, S. M., Chung, H., et al. (2009). Cellular uptake mechanism and intracellular fate of hydrophobically modified glycol chitosan nanoparticles. Journal of Controlled Release, 135(3), 259-267. doi: 10. 1016/j. jconrel. 2009. 01. 018.
-
(2009)
Journal of Controlled Release
, vol.135
, Issue.3
, pp. 259-267
-
-
Nam, H.Y.1
Kwon, S.M.2
Chung, H.3
-
203
-
-
77952917129
-
Doxorubicin-incorporated nanoparticles composed of poly(ethylene glycol)-grafted carboxymethyl chitosan and antitumor activity against glioma cells in vitro
-
doi:10.1016/j.colsurfb.2010.03.037
-
Jeong, Y. I., Jin, S. G., Kim, I. Y., et al. (2010). Doxorubicin-incorporated nanoparticles composed of poly(ethylene glycol)-grafted carboxymethyl chitosan and antitumor activity against glioma cells in vitro. Colloids and Surfaces B, 79(1), 149-155. doi: 10. 1016/j. colsurfb. 2010. 03. 037.
-
(2010)
Colloids and Surfaces B
, vol.79
, Issue.1
, pp. 149-155
-
-
Jeong, Y.I.1
Jin, S.G.2
Kim, I.Y.3
-
204
-
-
0025357359
-
Tissue distribution of doxorubicin associated with polyhexylcyanoacrylate nanoparticles
-
doi:10.1007/BF0294028
-
Verdun, C., Brasseur, F., Vranckx, H., Couvreur, P., Roland, M. (1990). Tissue distribution of doxorubicin associated with polyhexylcyanoacrylate nanoparticles. Cancer Chemotherapy and Pharmacology, 26(1), 13-18. doi: 10. 1007/BF0294028.
-
(1990)
Cancer Chemotherapy and Pharmacology
, vol.26
, Issue.1
, pp. 13-18
-
-
Verdun, C.1
Brasseur, F.2
Vranckx, H.3
Couvreur, P.4
Roland, M.5
-
205
-
-
0029379537
-
Surface modification of nanoparticles to oppose uptake by the mononuclear phagocyte system
-
doi:10.1016/0169-409X(95)00039-A
-
Storm, G., Belliot, S., Daemen, T., Lasic, D. (1995). Surface modification of nanoparticles to oppose uptake by the mononuclear phagocyte system. Advanced Drug Delivery Reviews, 17, 31-48. doi: 10. 1016/0169-409X(95)00039-A.
-
(1995)
Advanced Drug Delivery Reviews
, vol.17
, pp. 31-48
-
-
Storm, G.1
Belliot, S.2
Daemen, T.3
Lasic, D.4
-
206
-
-
0026122420
-
Protein-surface interactions in the presence of polyethylene oxide: I. Simplified theory
-
doi:10.1016/0021-9797(91)90043-8
-
Jeon, S. I., Lee, J. H., Andrade, J. D., De Gennes, P. G. (1991). Protein-surface interactions in the presence of polyethylene oxide: I. Simplified theory. Journal of Colloid and Interface Science, 142, 149-158. doi: 10. 1016/0021-9797(91)90043-8.
-
(1991)
Journal of Colloid and Interface Science
, vol.142
, pp. 149-158
-
-
Jeon, S.I.1
Lee, J.H.2
Andrade, J.D.3
de Gennes, P.G.4
-
207
-
-
0033751962
-
Design of folic acid-conjugated nanoparticles for drug targeting
-
doi:10.1002/1520-6017(200011)89:11<1452::AID-JPS8>3.0.CO;2-P
-
Stella, B., Arpicco, S., Peracchia, M., Desmaele, D., Hoebeke, J., Renoir, M., Angelo, J., Cattel, L., Couvreur, P. (2000). Design of folic acid-conjugated nanoparticles for drug targeting. Journal of Pharmaceutical Sciences, 89(11), 1452-1464. doi: 10. 1002/1520-6017(200011)89: 11< 1452:: AID-JPS8> 3. 0. CO; 2-P.
-
(2000)
Journal of Pharmaceutical Sciences
, vol.89
, Issue.11
, pp. 1452-1464
-
-
Stella, B.1
Arpicco, S.2
Peracchia, M.3
Desmaele, D.4
Hoebeke, J.5
Renoir, M.6
Angelo, J.7
Cattel, L.8
Couvreur, P.9
-
208
-
-
0034104453
-
Resistance mechanisms associated with altered intracellular distribution of anticancer agents
-
doi:10.1016/S0163-7258(99)00073-X
-
Larsen, A. K., Escargueil, A. E., Skladanowski, A. (2000). Resistance mechanisms associated with altered intracellular distribution of anticancer agents. Pharmacology and Therapeutics, 85(3), 217-229. doi: 10. 1016/S0163-7258(99)00073-X.
-
(2000)
Pharmacology and Therapeutics
, vol.85
, Issue.3
, pp. 217-229
-
-
Larsen, A.K.1
Escargueil, A.E.2
Skladanowski, A.3
-
209
-
-
0028036158
-
Enhanced cytotoxicity of doxorubicin encapsulated in polyisohexylcyanoacrylate nanospheres against multidrug-resistant tumour cells in culture
-
Bennis, S., Chapey, C., Couvreur, P., Robert, J. (1994). Enhanced cytotoxicity of doxorubicin encapsulated in polyisohexylcyanoacrylate nanospheres against multidrug-resistant tumour cells in culture. European Journal of Cancer, 30A(1), 89-93.
-
(1994)
European Journal of Cancer
, vol.30 A
, Issue.1
, pp. 89-93
-
-
Bennis, S.1
Chapey, C.2
Couvreur, P.3
Robert, J.4
-
210
-
-
0025091427
-
Nanocapsules as carriers for oral peptide delivery
-
doi:10.1016/0168-3659(90)90013-J
-
Damge, C., Michel, C., Aprahamian, M., Couvreur, P., Devissaguet, J. P. (1990). Nanocapsules as carriers for oral peptide delivery. Journal of Controlled Release, 13, 233-239. doi: 10. 1016/0168-3659(90)90013-J.
-
(1990)
Journal of Controlled Release
, vol.13
, pp. 233-239
-
-
Damge, C.1
Michel, C.2
Aprahamian, M.3
Couvreur, P.4
Devissaguet, J.P.5
-
211
-
-
0031064049
-
Mucosal immunity-a major adaptive defense mechanism
-
Brandtzaeg, P., Berstad, A., Farstad, I., Haraldsen, G., Helgeland, L., Jahnsen, F., Johansen, F., Natvig, I., Nilsen, E., Rugtveit, J. (1997). Mucosal immunity-a major adaptive defense mechanism. Behring Institute Mitteilungen, 98(1), 1-23.
-
(1997)
Behring Institute Mitteilungen
, vol.98
, Issue.1
, pp. 1-23
-
-
Brandtzaeg, P.1
Berstad, A.2
Farstad, I.3
Haraldsen, G.4
Helgeland, L.5
Jahnsen, F.6
Johansen, F.7
Natvig, I.8
Nilsen, E.9
Rugtveit, J.10
-
212
-
-
0034996764
-
Long-circulating and target-specific nanoparticles: theory to practice
-
doi:0031-6997/01/5302-283-318$3.00
-
Moghimi, S. M., Hunter, A. C., Murray, J. C. (2001). Long-circulating and target-specific nanoparticles: theory to practice. Pharmacological Reviews, 53, 283-318. doi: 0031-6997/01/5302-283-318$3. 00.
-
(2001)
Pharmacological Reviews
, vol.53
, pp. 283-318
-
-
Moghimi, S.M.1
Hunter, A.C.2
Murray, J.C.3
-
213
-
-
0032482152
-
Temperature-responsive gels and thermogelling polymer matrices for protein and peptide delivery
-
doi:10.1016/S0169-409X(97)00121-X
-
Bromberg, L. E., Ron, E. S. (1998). Temperature-responsive gels and thermogelling polymer matrices for protein and peptide delivery. Advanced Drug Delivery Reviews, 31(3), 197-221. doi: 10. 1016/S0169-409X(97)00121-X.
-
(1998)
Advanced Drug Delivery Reviews
, vol.31
, Issue.3
, pp. 197-221
-
-
Bromberg, L.E.1
Ron, E.S.2
-
214
-
-
0031398518
-
Lectins and bacterial invasion factors for controlling endo- and transcytosis of bioadhesive drug carrier systems
-
Haltner, E., Easson, J., Lehr, C. (1997). Lectins and bacterial invasion factors for controlling endo- and transcytosis of bioadhesive drug carrier systems. European Journal of Pharmaceutics and Biopharmaceutics, 44, 3-13.
-
(1997)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.44
, pp. 3-13
-
-
Haltner, E.1
Easson, J.2
Lehr, C.3
-
215
-
-
0030952669
-
Enhanced oral uptake of tomato lectin-conjugated nanoparticles in the rat
-
doi:10.1023/A:1012153011884
-
Hussain, N., Jani, P. U., Florence, A. T. (1997). Enhanced oral uptake of tomato lectin-conjugated nanoparticles in the rat. Pharmaceutical Research, 14(5), 613-618. doi: 10. 1023/A: 1012153011884.
-
(1997)
Pharmaceutical Research
, vol.14
, Issue.5
, pp. 613-618
-
-
Hussain, N.1
Jani, P.U.2
Florence, A.T.3
-
216
-
-
0032586956
-
Vitamin B12-mediated transport of nanoparticles across Caco-2 cells
-
doi:10.1016/S0378-5173(98)00394-9
-
Russell-Jones, G. J., Arthur, L., Walker, H. (1999). Vitamin B12-mediated transport of nanoparticles across Caco-2 cells. International Journal of Pharmaceutics, 179(2), 247-255. doi: 10. 1016/S0378-5173(98)00394-9.
-
(1999)
International Journal of Pharmaceutics
, vol.179
, Issue.2
, pp. 247-255
-
-
Russell-Jones, G.J.1
Arthur, L.2
Walker, H.3
-
217
-
-
68049144958
-
Specific targeting of brain tumors with an optical/magnetic resonance imaging nanoprobe across the blood-brain barrier
-
Veiseh, O., Sun, C., Fang, C., Bhattarai, N., Gunn, J., Kievit, F., Du, K., Pullar, B., Lee, D., Ellenbogen, R. G., Olson, J., Zhang, M. (2009). Specific targeting of brain tumors with an optical/magnetic resonance imaging nanoprobe across the blood-brain barrier. Cancer Research, 69, 6200-6207.
-
(2009)
Cancer Research
, vol.69
, pp. 6200-6207
-
-
Veiseh, O.1
Sun, C.2
Fang, C.3
Bhattarai, N.4
Gunn, J.5
Kievit, F.6
Du, K.7
Pullar, B.8
Lee, D.9
Ellenbogen, R.G.10
Olson, J.11
Zhang, M.12
-
218
-
-
57449121882
-
Getting into the brain: approaches to enhance brain drug delivery
-
doi:10.2165/0023210-200923010-00003
-
Patel, M. M., Goyal, B. R., Bhadada, S. V., Bhatt, J. S., Amin, A. F. (2009). Getting into the brain: approaches to enhance brain drug delivery. CNS Drugs, 23(1), 35-58. doi: 10. 2165/0023210-200923010-00003.
-
(2009)
CNS Drugs
, vol.23
, Issue.1
, pp. 35-58
-
-
Patel, M.M.1
Goyal, B.R.2
Bhadada, S.V.3
Bhatt, J.S.4
Amin, A.F.5
-
219
-
-
11944265265
-
Nanoparticle surface charges alter blood-brain barrier integrity and permeability
-
doi:10.1080/10611860400015936
-
Lockman, P. R., Koziara, J. M., Mumper, R. J., et al. (2004). Nanoparticle surface charges alter blood-brain barrier integrity and permeability. Journal of Drug Targeting, 12(9-10), 635-641. doi: 10. 1080/10611860400015936.
-
(2004)
Journal of Drug Targeting
, vol.12
, Issue.9-10
, pp. 635-641
-
-
Lockman, P.R.1
Koziara, J.M.2
Mumper, R.J.3
-
220
-
-
26944477353
-
Peptide-derivatized biodegradable nanoparticles able to cross the blood-brain barrier
-
doi:10.1016/j.jconrel.2005.07.013
-
Costantino, L., Gandolfi, F., Tosi, G., Rivasi, F., Vandelli, M. A., Forni, F. (2005). Peptide-derivatized biodegradable nanoparticles able to cross the blood-brain barrier. Journal of Controlled Release, 108(1), 84-96. doi: 10. 1016/j. jconrel. 2005. 07. 013.
-
(2005)
Journal of Controlled Release
, vol.108
, Issue.1
, pp. 84-96
-
-
Costantino, L.1
Gandolfi, F.2
Tosi, G.3
Rivasi, F.4
Vandelli, M.A.5
Forni, F.6
-
221
-
-
78650680356
-
Brain targeting with surface-modified poly(d, l-lactic-co-glycolic acid) nanoparticles delivered via carotid artery administration
-
doi:10.1016/j.ejpb.2010.11.002
-
Tahara, K., Miyazaki, Y., Kawashima, Y., Kreuter, J., Yamamoto, H. (2011). Brain targeting with surface-modified poly(d, l-lactic-co-glycolic acid) nanoparticles delivered via carotid artery administration. European Journal of Pharmaceutics and Biopharmaceutics, 77(1), 84-88. doi: 10. 1016/j. ejpb. 2010. 11. 002.
-
(2011)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.77
, Issue.1
, pp. 84-88
-
-
Tahara, K.1
Miyazaki, Y.2
Kawashima, Y.3
Kreuter, J.4
Yamamoto, H.5
-
222
-
-
40949127319
-
Therapeutic nanoparticles for drug delivery in cancer
-
doi:10.1158/1078-0432.CCR-07-1441
-
Cho, K., Wang, X., Nie, S., et al. (2008). Therapeutic nanoparticles for drug delivery in cancer. Clinicalo Cancer Research, 14(5), 1310-1316. doi: 10. 1158/1078-0432. CCR-07-1441.
-
(2008)
Clinicalo Cancer Research
, vol.14
, Issue.5
, pp. 1310-1316
-
-
Cho, K.1
Wang, X.2
Nie, S.3
|